SNP Detail Info-rs9584217

Organism: Homo sapiens

Alleles: C>G

Gene : Feature

None

p-value: Check p-value

Variation Type: SNV (Single Nucleotide Variation)

Frequency:

G=0159 (4768/29940,GnomAD)
G=0204 (5960/29118,TOPMED)
G=0157 (785/5008,1000G)
G=0106 (408/3854,ALSPAC)
G=0103 (383/3708,TWINSUK)

Position: chr13:87069909 (GRCh38.p7) (13q31.1)

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 13	NC_000013.11:g.87069909C>G
GRCh37.p13 chr 13	NC_000013.10:g.87722164C>G

Study	Population	Group	Sample #	Ref Allele	Alt Allele
1000Genomes	African	Sub	1322	C=0.628	G=0.372
1000Genomes	American	Sub	694	C=0.900	G=0.100
1000Genomes	East Asian	Sub	1008	C=0.970	G=0.030
1000Genomes	Europe	Sub	1006	C=0.906	G=0.094
1000Genomes	Global	Study-wide	5008	C=0.843	G=0.157
1000Genomes	South Asian	Sub	978	C=0.900	G=0.100
The Avon Longitudinal Study of Parents and Children	PARENT AND CHILD COHORT	Study-wide	3854	C=0.894	G=0.106
The Genome Aggregation Database	African	Sub	8716	C=0.657	G=0.343
The Genome Aggregation Database	American	Sub	838	C=0.930	G=0.070
The Genome Aggregation Database	East Asian	Sub	1618	C=0.954	G=0.046
The Genome Aggregation Database	Europe	Sub	18466	C=0.913	G=0.086
The Genome Aggregation Database	Global	Study-wide	29940	C=0.840	G=0.159
The Genome Aggregation Database	Other	Sub	302	C=0.840	G=0.160
Trans-Omics for Precision Medicine	Global	Study-wide	29118	C=0.795	G=0.204
UK 10K study - Twins	TWIN COHORT	Study-wide	3708	C=0.897	G=0.103

rs9584217