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rs959695

From SNPedia

Orientationminus
Stabilizedminus
Make rs959695(A;A)
Make rs959695(A;G)
Make rs959695(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position99822954
GeneVPS13B
is asnp
is mentioned by
dbSNPrs959695
ebirs959695
HLIrs959695
Exacrs959695
Varsomers959695
Maprs959695
PheGenIrs959695
hapmaprs959695
1000 genomesrs959695
hgdprs959695
ensemblrs959695
gopubmedrs959695
geneviewrs959695
scholarrs959695
googlers959695
pharmgkbrs959695
gwascentralrs959695
openSNPrs959695
23andMers959695
23andMe allrs959695
SNP Nexus

SNPshotrs959695
SNPdbers959695
MSV3drs959695
GWAS Ctlgrs959695
GMAF0.4137
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22745009OA-icon.png]
Trait
Title Multiple loci influencing hippocampal degeneration identified by genome scan.
Risk Allele C
P-val 0.000001
Odds Ratio None None