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rs794728625

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728625(A;A)
Make rs794728625(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807228
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728625
ebirs794728625
HLIrs794728625
Exacrs794728625
Varsomers794728625
Maprs794728625
PheGenIrs794728625
hapmaprs794728625
1000 genomesrs794728625
hgdprs794728625
ensemblrs794728625
gopubmedrs794728625
geneviewrs794728625
scholarrs794728625
googlers794728625
pharmgkbrs794728625
gwascentralrs794728625
openSNPrs794728625
23andMers794728625
23andMe allrs794728625
SNP Nexus

SNPshotrs794728625
SNPdbers794728625
MSV3drs794728625
GWAS Ctlgrs794728625
Max Magnitude0
ClinVar
Risk rs794728625(A;A)
Alt rs794728625(A;A)
Reference rs794728625(G;G)
Significance Pathogenic
Disease not provided Multiple endocrine neoplasia
Variation info
Gene MEN1
CLNDBN not provided Multiple endocrine neoplasia, type 1
Reversed 1
HGVS NC_000011.9:g.64574700C>T
CLNSRC
CLNACC RCV000182415.1, RCV000205749.1,