#URL	https://www.ncbi.nlm.nih.gov/snp/rs269/download/frequency
#NCBI Reference SNP (rs) Report ALPHA	rs269
#Current Build	156
#Released	October 14, 2022
#Organism	Homo sapiens
#Position	chr8:19956156 (GRCh38.p14)
#Alleles	T>A / T>G
#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	T=0.729434	G=0.270566	PRJNA400167	
Allele Frequency Aggregator	Total	Global	31584	T=0.83245	A=0.00000, G=0.16755	PRJNA507278	SAMN10492705
Allele Frequency Aggregator	European	Sub	26288	T=0.84898	A=0.00000, G=0.15102		SAMN10492695
Allele Frequency Aggregator	African	Sub	2734	T=0.6697	A=0.0000, G=0.3303		SAMN10492703
Allele Frequency Aggregator	Other	Sub	1734	T=0.7912	A=0.0000, G=0.2088		SAMN11605645
Allele Frequency Aggregator	Latin American 2	Sub	540	T=0.944	A=0.000, G=0.056		SAMN10492700
Allele Frequency Aggregator	Latin American 1	Sub	130	T=0.915	A=0.000, G=0.085		SAMN10492699
Allele Frequency Aggregator	South Asian	Sub	86	T=0.91	A=0.00, G=0.09		SAMN10492702
Allele Frequency Aggregator	Asian	Sub	72	T=0.89	A=0.00, G=0.11		SAMN10492704
14KJPN	JAPANESE	Study-wide	28258	T=0.78406	G=0.21594	PRJNA678214	SAMN16789458
8.3KJPN	JAPANESE	Study-wide	16760	T=0.78174	G=0.21826	PRJNA678214	SAMN16789458
1000Genomes_30x	Global	Study-wide	6404	T=0.7117	G=0.2883	PRJEB31736	SAMN07490465
1000Genomes_30x	African	Sub	1786	T=0.5157	G=0.4843		SAMN07486022
1000Genomes_30x	Europe	Sub	1266	T=0.7891	G=0.2109		SAMN07488239
1000Genomes_30x	South Asian	Sub	1202	T=0.8128	G=0.1872		SAMN07486027
1000Genomes_30x	East Asian	Sub	1170	T=0.7504	G=0.2496		SAMN07486024
1000Genomes_30x	American	Sub	980	T=0.799	G=0.201		SAMN07488242
1000Genomes	Global	Study-wide	5008	T=0.7220	G=0.2780	PRJEB6930	SAMN07490465
1000Genomes	African	Sub	1322	T=0.5295	G=0.4705		SAMN07486022
1000Genomes	East Asian	Sub	1008	T=0.7540	G=0.2460		SAMN07486024
1000Genomes	Europe	Sub	1006	T=0.8012	G=0.1988		SAMN07488239
1000Genomes	South Asian	Sub	978	T=0.812	G=0.188		SAMN07486027
1000Genomes	American	Sub	694	T=0.801	G=0.199		SAMN07488242
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.8438	G=0.1562	PRJNA489787	
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.8181	G=0.1819	PRJEB7217	
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.8118	G=0.1882	PRJEB7218	
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.7922	G=0.2078	PRJNA589833	
HapMap	Global	Study-wide	1892	T=0.6845	G=0.3155	PRJNA60817	SAMN10820145
HapMap	American	Sub	770	T=0.775	G=0.225		SAMN10821182
HapMap	African	Sub	692	T=0.533	G=0.467		SAMN10821181
HapMap	Asian	Sub	254	T=0.780	G=0.220		SAMN10821184
HapMap	Europe	Sub	176	T=0.744	G=0.256		SAMN10821183
Korean Genome Project	KOREAN	Study-wide	1832	T=0.8051	G=0.1949	PRJNA609628	
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.818	G=0.182	PRJEB5829	SAMN13000132
Northern Sweden	ACPOP	Study-wide	600	T=0.860	G=0.140	PPRJNA503394	SAMN10359154
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.770	G=0.230	PRJEB8705	SAMN13001620
SGDP_PRJ	Global	Study-wide	224	T=0.388	G=0.612	PRJNA586841	
Qatari	Global	Study-wide	216	T=0.778	G=0.222	PRJNA288297	SAMN13019808
A Vietnamese Genetic Variation Database	Global	Study-wide	216	T=0.787	G=0.213	PRJNA515199	SAMN10744005
Ancient Sardinia genome-wide 1240k capture data generation and analysis	Global	Study-wide	84	T=0.76	G=0.24	PRJEB36033	SAMN15458807
The Danish reference pan genome	Danish	Study-wide	40	T=0.85	G=0.15	PRJEB7725	SAMN13003120
Siberian	Global	Study-wide	16	T=0.50	G=0.50	PRJNA267856	SAMN13113809