SNP Detail Info-rs9537050

Organism: Homo sapiens

Alleles: A>G / A>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0112 (3367/29952,GnomAD)
G=0134 (3916/29116,TOPMED)
G=0138 (691/5008,1000G)
G=0060 (231/3854,ALSPAC)
G=0070 (258/3708,TWINSUK)

Position: chr13:55278916 (GRCh38.p7) (13q21.1)

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	A=0.775	G=0.225
1000Genomes	American	Sub	694	A=0.780	G=0.220
1000Genomes	East Asian	Sub	1008	A=0.905	G=0.095
1000Genomes	Europe	Sub	1006	A=0.949	G=0.051
1000Genomes	Global	Study-wide	5008	A=0.862	G=0.138
1000Genomes	South Asian	Sub	978	A=0.900	G=0.100
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	A=0.940	G=0.060
The Genome Aggregation Database	African	Sub	8712	A=0.797	T=0.000
The Genome Aggregation Database	American	Sub	838	A=0.770	T=0.00,
The Genome Aggregation Database	East Asian	Sub	1610	A=0.906	T=0.001
The Genome Aggregation Database	Europe	Sub	18490	A=0.932	T=0.000
The Genome Aggregation Database	Global	Study-wide	29952	A=0.887	T=0.000
The Genome Aggregation Database	Other	Sub	302	A=0.970	T=0.00,
Trans-Omics for Precision Medicine	Global	Study-wide	29116	A=0.865	G=0.134
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	A=0.930	G=0.070

rs9537050