SNP Detail Info-rs9874932

Organism: Homo sapiens

Alleles: G>A / G>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

A=0197 (5903/29898,GnomAD)
A=0271 (7901/29118,TOPMED)
A=0215 (1076/5008,1000G)
A=0104 (400/3854,ALSPAC)
A=0108 (399/3708,TWINSUK)

Position: chr3:164838860 (GRCh38.p7) (3q26.1)

Phenotype: AD

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	G=0.483	A=0.517
1000Genomes	American	Sub	694	G=0.900	A=0.100
1000Genomes	East Asian	Sub	1008	G=0.902	A=0.098
1000Genomes	Europe	Sub	1006	G=0.906	A=0.094
1000Genomes	Global	Study-wide	5008	G=0.785	A=0.215
1000Genomes	South Asian	Sub	978	G=0.870	A=0.130
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	G=0.896	A=0.104
The Genome Aggregation Database	African	Sub	8678	G=0.539	A=0.461
The Genome Aggregation Database	American	Sub	838	G=0.930	A=0.07,
The Genome Aggregation Database	East Asian	Sub	1612	G=0.890	A=0.110
The Genome Aggregation Database	Europe	Sub	18470	G=0.911	A=0.088
The Genome Aggregation Database	Global	Study-wide	29898	G=0.802	A=0.197
The Genome Aggregation Database	Other	Sub	300	G=0.910	A=0.09,
Trans-Omics for Precision Medicine	Global	Study-wide	29118	G=0.728	A=0.271
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	G=0.892	A=0.108

rs9874932