SNP Detail Info-rs8126263

Organism: Homo sapiens

Alleles: C>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

T=0112 (3361/29970,GnomAD)
T=0097 (2841/29118,TOPMED)
T=0150 (752/5008,1000G)
T=0105 (403/3854,ALSPAC)
T=0117 (432/3708,TWINSUK)

Position: chr20:23785640 (GRCh38.p7) (20p11.21)

Phenotype: AD

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 20	NC_000020.11:g.23785640C>T
GRCh37.p13 chr 20	NC_000020.10:g.23766277C>T

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	C=0.950	T=0.050
1000Genomes	American	Sub	694	C=0.720	T=0.280
1000Genomes	East Asian	Sub	1008	C=0.714	T=0.286
1000Genomes	Europe	Sub	1006	C=0.862	T=0.138
1000Genomes	Global	Study-wide	5008	C=0.850	T=0.150
1000Genomes	South Asian	Sub	978	C=0.930	T=0.070
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.895	T=0.105
The Genome Aggregation Database	African	Sub	8722	C=0.946	T=0.054
The Genome Aggregation Database	American	Sub	836	C=0.720	T=0.280
The Genome Aggregation Database	East Asian	Sub	1614	C=0.725	T=0.275
The Genome Aggregation Database	Europe	Sub	18496	C=0.881	T=0.118
The Genome Aggregation Database	Global	Study-wide	29970	C=0.887	T=0.112
The Genome Aggregation Database	Other	Sub	302	C=0.900	T=0.100
Trans-Omics for Precision Medicine	Global	Study-wide	29118	C=0.902	T=0.097
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.883	T=0.117

rs8126263