SNP Detail Info-rs9819217

Organism: Homo sapiens

Alleles: C>T

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

T=0130 (3896/29926,GnomAD)
T=0164 (4778/29118,TOPMED)
T=0139 (697/5008,1000G)
T=0104 (399/3854,ALSPAC)
T=0106 (392/3708,TWINSUK)

Position: chr3:164847975 (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

Sequence Name	Change(s)
GRCh38.p7 chr 3	NC_000003.12:g.164847975C>T
GRCh37.p13 chr 3	NC_000003.11:g.164565763C>T

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	C=0.755	T=0.245
1000Genomes	American	Sub	694	C=0.920	T=0.080
1000Genomes	East Asian	Sub	1008	C=0.905	T=0.095
1000Genomes	Europe	Sub	1006	C=0.907	T=0.093
1000Genomes	Global	Study-wide	5008	C=0.861	T=0.139
1000Genomes	South Asian	Sub	978	C=0.870	T=0.130
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.896	T=0.104
The Genome Aggregation Database	African	Sub	8720	C=0.767	T=0.233
The Genome Aggregation Database	American	Sub	836	C=0.940	T=0.060
The Genome Aggregation Database	East Asian	Sub	1612	C=0.898	T=0.102
The Genome Aggregation Database	Europe	Sub	18456	C=0.912	T=0.087
The Genome Aggregation Database	Global	Study-wide	29926	C=0.869	T=0.130
The Genome Aggregation Database	Other	Sub	302	C=0.910	T=0.090
Trans-Omics for Precision Medicine	Global	Study-wide	29118	C=0.835	T=0.164
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.894	T=0.106

rs9819217