SNP Detail Info-rs1120839

Organism: Homo sapiens

Alleles: G>A

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G==0104 (3139/29940,GnomAD)
G==0089 (2596/29118,TOPMED)
G==0174 (870/5008,1000G)
G==0079 (306/3854,ALSPAC)
G==0078 (290/3708,TWINSUK)

Position: chr21:25442104 (GRCh38.p7) (21q21.2)

Phenotype: ND

Dataset:

GWASdb2

Publications: 1 publication(s)

Genomic View: See rs on genome

Enhancer: 0 Enhancer around

Promoter: 0 Promoter around

Sequence Name	Change(s)
GRCh38.p7 chr 21	NC_000021.9:g.25442104G>A
GRCh37.p13 chr 21	NC_000021.8:g.26814416G>A

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	G=0.136	A=0.864
1000Genomes	American	Sub	694	G=0.030	A=0.970
1000Genomes	East Asian	Sub	1008	G=0.413	A=0.587
1000Genomes	Europe	Sub	1006	G=0.083	A=0.917
1000Genomes	Global	Study-wide	5008	G=0.174	A=0.826
1000Genomes	South Asian	Sub	978	G=0.170	A=0.830
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.079	A=0.921
Trans-Omics for Precision Medicine	Global	Study-wide	29118	G=0.089	A=0.910
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.078	A=0.922

rs1120839