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rs5993891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs5993891(C;T)
Make rs5993891(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19972223
GeneARVCF
is asnp
is mentioned by
dbSNPrs5993891
ebirs5993891
HLIrs5993891
Exacrs5993891
Varsomers5993891
Maprs5993891
PheGenIrs5993891
hapmaprs5993891
1000 genomesrs5993891
hgdprs5993891
ensemblrs5993891
gopubmedrs5993891
geneviewrs5993891
scholarrs5993891
googlers5993891
pharmgkbrs5993891
gwascentralrs5993891
openSNPrs5993891
23andMers5993891
23andMe allrs5993891
SNP Nexus

SNPshotrs5993891
SNPdbers5993891
MSV3drs5993891
GWAS Ctlgrs5993891
GMAF0.1272
Max Magnitude0
? (C;C) (C;T) (T;T) 28
rs5993891 is a SNP in the armadillo repeat gene deleted in velocardiofacial syndrome ARVCF gene - how's that for a gene name?

This SNP is one of five SNPs reported to be useful in a SNP set defining the risk of dying from prostate cancer among patients with the disease; see gs242 and gs243.