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rs794728638

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728638(-;T)
Make rs794728638(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64809962
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728638
ClinGenrs794728638
ebirs794728638
HLIrs794728638
Exacrs794728638
Varsomers794728638
Maprs794728638
PheGenIrs794728638
hapmaprs794728638
1000 genomesrs794728638
hgdprs794728638
ensemblrs794728638
gopubmedrs794728638
geneviewrs794728638
scholarrs794728638
googlers794728638
pharmgkbrs794728638
gwascentralrs794728638
openSNPrs794728638
23andMers794728638
23andMe allrs794728638
SNP Nexus

SNPshotrs794728638
SNPdbers794728638
MSV3drs794728638
GWAS Ctlgrs794728638
Max Magnitude0
ClinVar
Risk rs794728638(T;T)
Alt rs794728638(T;T)
Reference Rs794728638(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577435dupA
CLNSRC
CLNACC RCV000182432.1,