#URL https://www.ncbi.nlm.nih.gov/snp/rs256/download/frequency #NCBI Reference SNP (rs) Report ALPHA rs256 #Current Build 156 #Released October 14, 2022 #Organism Homo sapiens #Position chr8:19954456 (GRCh38.p14) #Alleles C>T #Variation Type SNV (Single Nucleotide Variation) #Publications 2 citations # #Frequency Data Table ################# #Study Population Group Samplesize Ref Allele Alt Allele BioProject ID BioSample ID TopMed Global Study-wide 264690 C=0.877902 T=0.122098 PRJNA400167 Allele Frequency Aggregator Total Global 243892 C=0.855046 T=0.144954 PRJNA507278 SAMN10492705 Allele Frequency Aggregator European Sub 217418 C=0.854203 T=0.145797 SAMN10492695 Allele Frequency Aggregator Other Sub 8290 C=0.8513 T=0.1487 SAMN11605645 Allele Frequency Aggregator Latin American 2 Sub 6594 C=0.8450 T=0.1550 SAMN10492700 Allele Frequency Aggregator African Sub 6390 C=0.9423 T=0.0577 SAMN10492703 Allele Frequency Aggregator Asian Sub 3814 C=0.7787 T=0.2213 SAMN10492704 Allele Frequency Aggregator Latin American 1 Sub 1026 C=0.8830 T=0.1170 SAMN10492699 Allele Frequency Aggregator South Asian Sub 360 C=0.817 T=0.183 SAMN10492702 gnomAD - Genomes Global Study-wide 140192 C=0.880856 T=0.119144 PRJNA398795 SAMN07488253 gnomAD - Genomes European Sub 75934 C=0.86272 T=0.13728 SAMN10181265 gnomAD - Genomes African Sub 42018 C=0.93724 T=0.06276 SAMN07488254 gnomAD - Genomes American Sub 13646 C=0.84406 T=0.15594 SAMN07488255 gnomAD - Genomes Ashkenazi Jewish Sub 3320 C=0.8244 T=0.1756 SAMN07488252 gnomAD - Genomes East Asian Sub 3122 C=0.7867 T=0.2133 SAMN07488251 gnomAD - Genomes Other Sub 2152 C=0.8769 T=0.1231 SAMN07488248 The PAGE Study Global Study-wide 78698 C=0.88852 T=0.11148 PRJNA168052 SAMN10868975 The PAGE Study AfricanAmerican Sub 32514 C=0.93655 T=0.06345 SAMN10868721 The PAGE Study Mexican Sub 10808 C=0.85159 T=0.14841 SAMN10868735 The PAGE Study Asian Sub 8318 C=0.7973 T=0.2027 SAMN10868722 The PAGE Study PuertoRican Sub 7918 C=0.8836 T=0.1164 SAMN10868968 The PAGE Study NativeHawaiian Sub 4534 C=0.8712 T=0.1288 SAMN10868777 The PAGE Study Cuban Sub 4230 C=0.8589 T=0.1411 SAMN10868733 The PAGE Study Dominican Sub 3828 C=0.9094 T=0.0906 SAMN10868734 The PAGE Study CentralAmerican Sub 2450 C=0.8510 T=0.1490 SAMN10868729 The PAGE Study SouthAmerican Sub 1982 C=0.8557 T=0.1443 SAMN10868969 The PAGE Study NativeAmerican Sub 1260 C=0.8659 T=0.1341 SAMN10868739 The PAGE Study SouthAsian Sub 856 C=0.825 T=0.175 SAMN10868970 14KJPN JAPANESE Study-wide 28258 C=0.78339 T=0.21661 PRJNA678214 SAMN16789458 8.3KJPN JAPANESE Study-wide 16760 C=0.78091 T=0.21909 PRJNA678214 SAMN16789458 1000Genomes_30x Global Study-wide 6404 C=0.8546 T=0.1454 PRJEB31736 SAMN07490465 1000Genomes_30x African Sub 1786 C=0.9591 T=0.0409 SAMN07486022 1000Genomes_30x Europe Sub 1266 C=0.8397 T=0.1603 SAMN07488239 1000Genomes_30x South Asian Sub 1202 C=0.8228 T=0.1772 SAMN07486027 1000Genomes_30x East Asian Sub 1170 C=0.7513 T=0.2487 SAMN07486024 1000Genomes_30x American Sub 980 C=0.846 T=0.154 SAMN07488242 1000Genomes Global Study-wide 5008 C=0.8558 T=0.1442 PRJEB6930 SAMN07490465 1000Genomes African Sub 1322 C=0.9599 T=0.0401 SAMN07486022 1000Genomes East Asian Sub 1008 C=0.7550 T=0.2450 SAMN07486024 1000Genomes Europe Sub 1006 C=0.8529 T=0.1471 SAMN07488239 1000Genomes South Asian Sub 978 C=0.823 T=0.177 SAMN07486027 1000Genomes American Sub 694 C=0.854 T=0.146 SAMN07488242 Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.8705 T=0.1295 PRJNA489787 The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.8552 T=0.1448 PRJEB7217 UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.8557 T=0.1443 PRJEB7218 KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.7904 T=0.2096 PRJNA589833 Korean Genome Project KOREAN Study-wide 1832 C=0.8057 T=0.1943 PRJNA609628 Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.853 T=0.147 PRJEB5829 SAMN13000132 CNV burdens in cranial meningiomas Global Study-wide 788 C=0.811 T=0.189 PRJEB37584 SAMN15458720 CNV burdens in cranial meningiomas CRM Sub 788 C=0.811 T=0.189 SAMN15458720 Northern Sweden ACPOP Study-wide 600 C=0.885 T=0.115 PPRJNA503394 SAMN10359154 HapMap Global Study-wide 320 C=0.884 T=0.116 PRJNA60817 SAMN10820145 HapMap African Sub 118 C=0.983 T=0.017 SAMN10821181 HapMap American Sub 116 C=0.862 T=0.138 SAMN10821182 HapMap Asian Sub 86 C=0.78 T=0.22 SAMN10821184 Qatari Global Study-wide 216 C=0.894 T=0.106 PRJNA288297 SAMN13019808 A Vietnamese Genetic Variation Database Global Study-wide 214 C=0.794 T=0.206 PRJNA515199 SAMN10744005 SGDP_PRJ Global Study-wide 152 C=0.408 T=0.592 PRJNA586841 The Danish reference pan genome Danish Study-wide 40 C=0.85 T=0.15 PRJEB7725 SAMN13003120 Siberian Global Study-wide 16 C=0.50 T=0.50 PRJNA267856 SAMN13113809