#URL	https://www.ncbi.nlm.nih.gov/snp/rs385955/download/frequency
#NCBI Reference SNP (rs) Report ALPHA	rs385955
#Current Build	156
#Released	October 13, 2022
#Organism	Homo sapiens
#Position	chr6:2836032 (GRCh38.p14)
#Alleles	T>A / T>C / 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=0.443749	A=0.556251	PRJNA400167	
Allele Frequency Aggregator	Total	Global	39856	T=0.46257	A=0.53743, G=0.00000	PRJNA507278	SAMN10492705
Allele Frequency Aggregator	European	Sub	31106	T=0.45445	A=0.54555, G=0.00000		SAMN10492695
Allele Frequency Aggregator	Other	Sub	6692	T=0.4357	A=0.5643, G=0.0000		SAMN11605645
Allele Frequency Aggregator	African	Sub	1508	T=0.7188	A=0.2812, G=0.0000		SAMN10492703
Allele Frequency Aggregator	Latin American 1	Sub	372	T=0.462	A=0.538, G=0.000		SAMN10492699
Allele Frequency Aggregator	Latin American 2	Sub	90	T=0.86	A=0.14, G=0.00		SAMN10492700
Allele Frequency Aggregator	Asian	Sub	74	T=0.53	A=0.47, G=0.00		SAMN10492704
Allele Frequency Aggregator	South Asian	Sub	14	T=0.86	A=0.14, G=0.00		SAMN10492702
GO Exome Sequencing Project	Global	Study-wide	13006	T=0.47401	A=0.52599	PRJNA192955	
GO Exome Sequencing Project	European American	Sub	8600	T=0.4248	A=0.5752		
GO Exome Sequencing Project	African American	Sub	4406	T=0.5701	A=0.4299		
1000Genomes_30x	Global	Study-wide	6404	T=0.4502	A=0.5498	PRJEB31736	SAMN07490465
1000Genomes_30x	African	Sub	1786	T=0.5487	A=0.4513		SAMN07486022
1000Genomes_30x	Europe	Sub	1266	T=0.4107	A=0.5893		SAMN07488239
1000Genomes_30x	South Asian	Sub	1202	T=0.4526	A=0.5474		SAMN07486027
1000Genomes_30x	East Asian	Sub	1170	T=0.4291	A=0.5709		SAMN07486024
1000Genomes_30x	American	Sub	980	T=0.344	A=0.656		SAMN07488242
1000Genomes	Global	Study-wide	5008	T=0.4501	A=0.5499	PRJEB6930	SAMN07490465
1000Genomes	African	Sub	1322	T=0.5499	A=0.4501		SAMN07486022
1000Genomes	East Asian	Sub	1008	T=0.4315	A=0.5685		SAMN07486024
1000Genomes	Europe	Sub	1006	T=0.4175	A=0.5825		SAMN07488239
1000Genomes	South Asian	Sub	978	T=0.447	A=0.553		SAMN07486027
1000Genomes	American	Sub	694	T=0.339	A=0.661		SAMN07488242
Genetic variation in the Estonian population	Estonian	Study-wide	4480	T=0.4636	A=0.5364	PRJNA489787	
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.4351	A=0.5649	PRJEB7217	
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.4086	A=0.5914	PRJEB7218	
KOREAN population from KRGDB	KOREAN	Study-wide	2930	T=0.4034	A=0.5966, C=0.0000, G=0.0000	PRJNA589833	
Genome of the Netherlands Release 5	Genome of the Netherlands	Study-wide	998	T=0.415	A=0.585	PRJEB5829	SAMN13000132
A Vietnamese Genetic Variation Database	Global	Study-wide	613	T=0.493	A=0.507	PRJNA515199	SAMN10744005
Northern Sweden	ACPOP	Study-wide	600	T=0.495	A=0.505	PPRJNA503394	SAMN10359154
Medical Genome Project healthy controls from Spanish population	Spanish controls	Study-wide	534	T=0.421	A=0.579	PRJEB8705	SAMN13001620
SGDP_PRJ	Global	Study-wide	496	T=0.276	A=0.724	PRJNA586841	
HapMap	Global	Study-wide	308	T=0.458	A=0.542	PRJNA60817	SAMN10820145
HapMap	American	Sub	116	T=0.362	A=0.638		SAMN10821182
HapMap	African	Sub	106	T=0.651	A=0.349		SAMN10821181
HapMap	Asian	Sub	86	T=0.35	A=0.65		SAMN10821184
FINRISK	Finnish from FINRISK project	Study-wide	304	T=0.556	A=0.444	PRJEB7895	SAMN13002954
Qatari	Global	Study-wide	216	T=0.407	A=0.593	PRJNA288297	SAMN13019808
The Danish reference pan genome	Danish	Study-wide	40	T=0.50	A=0.50	PRJEB7725	SAMN13003120
Siberian	Global	Study-wide	40	T=0.30	A=0.70	PRJNA267856	SAMN13113809