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rs794728627

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728627(C;G)
Make rs794728627(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805703
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728627
ebirs794728627
HLIrs794728627
Exacrs794728627
Varsomers794728627
Maprs794728627
PheGenIrs794728627
hapmaprs794728627
1000 genomesrs794728627
hgdprs794728627
ensemblrs794728627
gopubmedrs794728627
geneviewrs794728627
scholarrs794728627
googlers794728627
pharmgkbrs794728627
gwascentralrs794728627
openSNPrs794728627
23andMers794728627
23andMe allrs794728627
SNP Nexus

SNPshotrs794728627
SNPdbers794728627
MSV3drs794728627
GWAS Ctlgrs794728627
Max Magnitude0
ClinVar
Risk rs794728627(G;G)
Alt rs794728627(G;G)
Reference rs794728627(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64573175G>C
CLNSRC
CLNACC RCV000182417.1,