#URL	https://www.ncbi.nlm.nih.gov/snp/rs271/download/frequency
#NCBI Reference SNP (rs) Report ALPHA	rs271
#Current Build	156
#Released	October 14, 2022
#Organism	Homo sapiens
#Position	chr8:19956191 (GRCh38.p14)
#Alleles	G>A / G>T
#Variation Type	SNV (Single Nucleotide Variation)
#Publications	3 citations
#
#Frequency Data Table
#################
#Study	Population	Group	Samplesize	Ref Allele	Alt Allele	BioProject ID	BioSample ID
14KJPN	JAPANESE	Study-wide	28258	G=0.78434	A=0.21566	PRJNA678214	SAMN16789458
Allele Frequency Aggregator	Total	Global	25748	G=0.91405	A=0.08595, T=0.00000	PRJNA507278	SAMN10492705
Allele Frequency Aggregator	European	Sub	15464	G=0.90423	A=0.09577, T=0.00000		SAMN10492695
Allele Frequency Aggregator	African	Sub	5928	G=0.9678	A=0.0322, T=0.0000		SAMN10492703
Allele Frequency Aggregator	Latin American 2	Sub	2604	G=0.8594	A=0.1406, T=0.0000		SAMN10492700
Allele Frequency Aggregator	Other	Sub	1300	G=0.8831	A=0.1169, T=0.0000		SAMN11605645
Allele Frequency Aggregator	Latin American 1	Sub	266	G=0.955	A=0.045, T=0.000		SAMN10492699
Allele Frequency Aggregator	Asian	Sub	98	G=0.93	A=0.07, T=0.00		SAMN10492704
Allele Frequency Aggregator	South Asian	Sub	88	G=0.95	A=0.05, T=0.00		SAMN10492702
8.3KJPN	JAPANESE	Study-wide	16760	G=0.78192	A=0.21808	PRJNA678214	SAMN16789458
1000Genomes_30x	Global	Study-wide	6404	G=0.8573	A=0.1427	PRJEB31736	SAMN07490465
1000Genomes_30x	African	Sub	1786	G=0.9608	A=0.0392		SAMN07486022
1000Genomes_30x	Europe	Sub	1266	G=0.8318	A=0.1682		SAMN07488239
1000Genomes_30x	South Asian	Sub	1202	G=0.8428	A=0.1572		SAMN07486027
1000Genomes_30x	East Asian	Sub	1170	G=0.7521	A=0.2479		SAMN07486024
1000Genomes_30x	American	Sub	980	G=0.845	A=0.155		SAMN07488242
1000Genomes	Global	Study-wide	5008	G=0.8580	A=0.1420	PRJEB6930	SAMN07490465
1000Genomes	African	Sub	1322	G=0.9607	A=0.0393		SAMN07486022
1000Genomes	East Asian	Sub	1008	G=0.7560	A=0.2440		SAMN07486024
1000Genomes	Europe	Sub	1006	G=0.8469	A=0.1531		SAMN07488239
1000Genomes	South Asian	Sub	978	G=0.839	A=0.161		SAMN07486027
1000Genomes	American	Sub	694	G=0.853	A=0.147		SAMN07488242
Genetic variation in the Estonian population	Estonian	Study-wide	4480	G=0.8596	A=0.1404	PRJNA489787	
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.8485	A=0.1515	PRJEB7217	
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.8503	A=0.1497	PRJEB7218	
KOREAN population from KRGDB	KOREAN	Study-wide	2930	G=0.7925	A=0.2075	PRJNA589833	
HapMap	Global	Study-wide	1892	G=0.8779	A=0.1221	PRJNA60817	SAMN10820145
HapMap	American	Sub	770	G=0.842	A=0.158		SAMN10821182
HapMap	African	Sub	692	G=0.965	A=0.035		SAMN10821181
HapMap	Asian	Sub	254	G=0.780	A=0.220		SAMN10821184
HapMap	Europe	Sub	176	G=0.835	A=0.165		SAMN10821183
Korean Genome Project	KOREAN	Study-wide	1832	G=0.8051	A=0.1949	PRJNA609628	
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	G=0.846	A=0.154	PRJEB5829	SAMN13000132
Chileans	Chilean	Study-wide	626	G=0.835	A=0.165	PRJNA577585	SAMN13030285
Northern Sweden	ACPOP	Study-wide	600	G=0.878	A=0.122	PPRJNA503394	SAMN10359154
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	G=0.833	A=0.167	PRJEB8705	SAMN13001620
Qatari	Global	Study-wide	216	G=0.894	A=0.106	PRJNA288297	SAMN13019808
A Vietnamese Genetic Variation Database	Global	Study-wide	214	G=0.785	A=0.215	PRJNA515199	SAMN10744005
SGDP_PRJ	Global	Study-wide	148	G=0.412	A=0.588	PRJNA586841	
The Danish reference pan genome	Danish	Study-wide	40	G=0.85	A=0.15	PRJEB7725	SAMN13003120
Siberian	Global	Study-wide	16	G=0.50	A=0.50	PRJNA267856	SAMN13113809