SNP Detail Info-rs576192

Organism: Homo sapiens

Alleles: T>A / T>G

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0455 (13625/29914,GnomAD)
T==0441 (12841/29118,TOPMED)
T==0353 (1769/5008,1000G)
G=0280 (1078/3854,ALSPAC)
G=0277 (1027/3708,TWINSUK)

Position: chr18:7519003 (GRCh38.p7) (18p11.23)

Phenotype: ND

Dataset:

GWASdb2

Publications: 1 publication(s)

Genomic View: See rs on genome

Enhancer: 0 Enhancer around

Promoter: 0 Promoter around

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	T=0.080	G=0.920
1000Genomes	American	Sub	694	T=0.560	G=0.440
1000Genomes	East Asian	Sub	1008	T=0.245	G=0.755
1000Genomes	Europe	Sub	1006	T=0.724	G=0.276
1000Genomes	Global	Study-wide	5008	T=0.353	G=0.647
1000Genomes	South Asian	Sub	978	T=0.310	G=0.690
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	T=0.720	G=0.280
The Genome Aggregation Database	African	Sub	8704	T=0.164	A=0.000
The Genome Aggregation Database	American	Sub	836	T=0.560	A=0.00,
The Genome Aggregation Database	East Asian	Sub	1618	T=0.219	A=0.000
The Genome Aggregation Database	Europe	Sub	18454	T=0.750	A=0.000
The Genome Aggregation Database	Global	Study-wide	29914	T=0.544	A=0.000
The Genome Aggregation Database	Other	Sub	302	T=0.650	A=0.00,
Trans-Omics for Precision Medicine	Global	Study-wide	29118	T=0.441	G=0.559
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	T=0.723	G=0.277

rs576192