SNP Detail Info-rs4761097

Organism: Homo sapiens

Alleles: G>A

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G==0448 (13394/29892,GnomAD)
G==0421 (12281/29118,TOPMED)
G==0408 (2044/5008,1000G)
G==0432 (1664/3854,ALSPAC)
G==0445 (1649/3708,TWINSUK)

Position: chr12:84793732 (GRCh38.p7) (12q21.31)

Phenotype: AD

Dataset:

GWASCatalog

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 12	NC_000012.12:g.84793732G>A
GRCh37.p13 chr 12	NC_000012.11:g.85187511G>A

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	G=0.453	A=0.547
1000Genomes	American	Sub	694	G=0.340	A=0.660
1000Genomes	East Asian	Sub	1008	G=0.213	A=0.787
1000Genomes	Europe	Sub	1006	G=0.460	A=0.540
1000Genomes	Global	Study-wide	5008	G=0.408	A=0.592
1000Genomes	South Asian	Sub	978	G=0.540	A=0.460
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.432	A=0.568
The Genome Aggregation Database	African	Sub	8694	G=0.458	A=0.542
The Genome Aggregation Database	American	Sub	838	G=0.340	A=0.660
The Genome Aggregation Database	East Asian	Sub	1620	G=0.231	A=0.769
The Genome Aggregation Database	Europe	Sub	18440	G=0.468	A=0.531
The Genome Aggregation Database	Global	Study-wide	29892	G=0.448	A=0.551
The Genome Aggregation Database	Other	Sub	300	G=0.390	A=0.610
Trans-Omics for Precision Medicine	Global	Study-wide	29118	G=0.421	A=0.578
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.445	A=0.555

PMID	Title	Author	Journal
23942779	A genome-wide association study of behavioral disinhibition.	McGue M	Behav Genet

SNP ID	p-value	Traits	Study
rs4761097	2E-06	alcohol dependence	23942779

Position (v37)	eGene	GeneID	Variant	p-value	TSS	Tissue
There is no eQTL annotation for this SNP

Probe ID	Position	Gene	beta	p-value
There is no meQTL annotation for this SNP

rs4761097