nih-gov/www.ncbi.nlm.nih.gov/snp/rs200/download/frequency
2025-03-17 02:05:34 +00:00

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#URL https://www.ncbi.nlm.nih.gov/snp/rs200/download/frequency
#NCBI Reference SNP (rs) Report ALPHA rs200
#Current Build 156
#Released October 14, 2022
#Organism Homo sapiens
#Position chr7:27907236 (GRCh38.p14)
#Alleles C>A / C>T
#Variation Type SNV (Single Nucleotide Variation)
#Publications 0 citations
#
#Frequency Data Table
#################
#Study Population Group Samplesize Ref Allele Alt Allele BioProject ID BioSample ID
TopMed Global Study-wide 264690 C=0.050334 T=0.949666 PRJNA400167
gnomAD - Genomes Global Study-wide 140208 C=0.048328 T=0.951672 PRJNA398795 SAMN07488253
gnomAD - Genomes European Sub 75936 C=0.06195 T=0.93805 SAMN10181265
gnomAD - Genomes African Sub 42012 C=0.01314 T=0.98686 SAMN07488254
gnomAD - Genomes American Sub 13652 C=0.07611 T=0.92389 SAMN07488255
gnomAD - Genomes Ashkenazi Jewish Sub 3324 C=0.1008 T=0.8992 SAMN07488252
gnomAD - Genomes East Asian Sub 3134 C=0.0000 T=1.0000 SAMN07488251
gnomAD - Genomes Other Sub 2150 C=0.0679 T=0.9321 SAMN07488248
14KJPN JAPANESE Study-wide 28258 C=0.00000 T=1.00000 PRJNA678214 SAMN16789458
Allele Frequency Aggregator Total Global 18890 C=0.05315 T=0.94685 PRJNA507278 SAMN10492705
Allele Frequency Aggregator European Sub 14286 C=0.06223 T=0.93777 SAMN10492695
Allele Frequency Aggregator African Sub 2946 C=0.0112 T=0.9888 SAMN10492703
Allele Frequency Aggregator Other Sub 692 C=0.056 T=0.944 SAMN11605645
Allele Frequency Aggregator Latin American 2 Sub 610 C=0.049 T=0.951 SAMN10492700
Allele Frequency Aggregator Latin American 1 Sub 146 C=0.082 T=0.918 SAMN10492699
Allele Frequency Aggregator Asian Sub 112 C=0.000 T=1.000 SAMN10492704
Allele Frequency Aggregator South Asian Sub 98 C=0.01 T=0.99 SAMN10492702
8.3KJPN JAPANESE Study-wide 16758 C=0.00000 T=1.00000 PRJNA678214 SAMN16789458
1000Genomes_30x Global Study-wide 6404 C=0.0275 T=0.9725 PRJEB31736 SAMN07490465
1000Genomes_30x African Sub 1786 C=0.0050 T=0.9950 SAMN07486022
1000Genomes_30x Europe Sub 1266 C=0.0861 T=0.9139 SAMN07488239
1000Genomes_30x South Asian Sub 1202 C=0.0108 T=0.9892 SAMN07486027
1000Genomes_30x East Asian Sub 1170 C=0.0017 T=0.9983 SAMN07486024
1000Genomes_30x American Sub 980 C=0.044 T=0.956 SAMN07488242
1000Genomes Global Study-wide 5008 C=0.0268 T=0.9732 PRJEB6930 SAMN07490465
1000Genomes African Sub 1322 C=0.0053 T=0.9947 SAMN07486022
1000Genomes East Asian Sub 1008 C=0.0020 T=0.9980 SAMN07486024
1000Genomes Europe Sub 1006 C=0.0825 T=0.9175 SAMN07488239
1000Genomes South Asian Sub 978 C=0.011 T=0.989 SAMN07486027
1000Genomes American Sub 694 C=0.045 T=0.955 SAMN07488242
Genetic variation in the Estonian population Estonian Study-wide 4480 C=0.0482 T=0.9518 PRJNA489787
The Avon Longitudinal Study of Parents and Children PARENT AND CHILD COHORT Study-wide 3854 C=0.0669 T=0.9331 PRJEB7217
UK 10K study - Twins TWIN COHORT Study-wide 3708 C=0.0720 T=0.9280 PRJEB7218
KOREAN population from KRGDB KOREAN Study-wide 2930 C=0.0000 A=0.0000, T=1.0000 PRJNA589833
Korean Genome Project KOREAN Study-wide 1832 C=0.0000 T=1.0000 PRJNA609628
Genome of the Netherlands Release 5 Genome of the Netherlands Study-wide 998 C=0.060 T=0.940 PRJEB5829 SAMN13000132
Northern Sweden ACPOP Study-wide 600 C=0.058 T=0.942 PPRJNA503394 SAMN10359154
SGDP_PRJ Global Study-wide 552 C=0.016 T=0.984 PRJNA586841
HapMap Global Study-wide 328 C=0.024 T=0.976 PRJNA60817 SAMN10820145
HapMap American Sub 120 C=0.067 T=0.933 SAMN10821182
HapMap African Sub 118 C=0.000 T=1.000 SAMN10821181
HapMap Asian Sub 90 C=0.00 T=1.00 SAMN10821184
Qatari Global Study-wide 216 C=0.125 T=0.875 PRJNA288297 SAMN13019808
A Vietnamese Genetic Variation Database Global Study-wide 210 C=0.000 T=1.000 PRJNA515199 SAMN10744005
Siberian Global Study-wide 56 C=0.07 T=0.93 PRJNA267856 SAMN13113809
The Danish reference pan genome Danish Study-wide 40 C=0.03 T=0.97 PRJEB7725 SAMN13003120