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rs1356888

From SNPedia

Orientationplus
Stabilizedplus
Make rs1356888(C;C)
Make rs1356888(C;T)
Make rs1356888(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position50288880
GeneNRXN1
is asnp
is mentioned by
dbSNPrs1356888
ebirs1356888
HLIrs1356888
Exacrs1356888
Varsomers1356888
Maprs1356888
PheGenIrs1356888
hapmaprs1356888
1000 genomesrs1356888
hgdprs1356888
ensemblrs1356888
gopubmedrs1356888
geneviewrs1356888
scholarrs1356888
googlers1356888
pharmgkbrs1356888
gwascentralrs1356888
openSNPrs1356888
23andMers1356888
23andMe allrs1356888
SNP Nexus

SNPshotrs1356888
SNPdbers1356888
MSV3drs1356888
GWAS Ctlgrs1356888
GMAF0.1488
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20834067OA-icon.png]
Trait
Title Joint influence of small-effect genetic variants on human longevity.
Risk Allele
P-val 0.000001
Odds Ratio None None