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rs794728617

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728617(A;A)
Make rs794728617(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64808072
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728617
ebirs794728617
HLIrs794728617
Exacrs794728617
Varsomers794728617
Maprs794728617
PheGenIrs794728617
hapmaprs794728617
1000 genomesrs794728617
hgdprs794728617
ensemblrs794728617
gopubmedrs794728617
geneviewrs794728617
scholarrs794728617
googlers794728617
pharmgkbrs794728617
gwascentralrs794728617
openSNPrs794728617
23andMers794728617
23andMe allrs794728617
SNP Nexus

SNPshotrs794728617
SNPdbers794728617
MSV3drs794728617
GWAS Ctlgrs794728617
Max Magnitude0
ClinVar
Risk rs794728617(A;A)
Alt rs794728617(A;A)
Reference rs794728617(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575544G>T
CLNSRC
CLNACC RCV000182405.1,