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rs794728621

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728621(A;A)
Make rs794728621(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807902
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728621
ebirs794728621
HLIrs794728621
Exacrs794728621
Varsomers794728621
Maprs794728621
PheGenIrs794728621
hapmaprs794728621
1000 genomesrs794728621
hgdprs794728621
ensemblrs794728621
gopubmedrs794728621
geneviewrs794728621
scholarrs794728621
googlers794728621
pharmgkbrs794728621
gwascentralrs794728621
openSNPrs794728621
23andMers794728621
23andMe allrs794728621
SNP Nexus

SNPshotrs794728621
SNPdbers794728621
MSV3drs794728621
GWAS Ctlgrs794728621
Max Magnitude0
ClinVar
Risk rs794728621(A;A)
Alt rs794728621(A;A)
Reference rs794728621(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.64575374C>T
CLNSRC
CLNACC RCV000182410.1, RCV000230442.1,