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rs794728623

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728623(C;G)
Make rs794728623(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807669
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728623
ebirs794728623
HLIrs794728623
Exacrs794728623
Varsomers794728623
Maprs794728623
PheGenIrs794728623
hapmaprs794728623
1000 genomesrs794728623
hgdprs794728623
ensemblrs794728623
gopubmedrs794728623
geneviewrs794728623
scholarrs794728623
googlers794728623
pharmgkbrs794728623
gwascentralrs794728623
openSNPrs794728623
23andMers794728623
23andMe allrs794728623
SNP Nexus

SNPshotrs794728623
SNPdbers794728623
MSV3drs794728623
GWAS Ctlgrs794728623
Max Magnitude0
ClinVar
Risk rs794728623(G;G)
Alt rs794728623(G;G)
Reference rs794728623(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575141G>C
CLNSRC
CLNACC RCV000182412.1,