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rs794728626

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728626(A;A)
Make rs794728626(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807089
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728626
ebirs794728626
HLIrs794728626
Exacrs794728626
Varsomers794728626
Maprs794728626
PheGenIrs794728626
hapmaprs794728626
1000 genomesrs794728626
hgdprs794728626
ensemblrs794728626
gopubmedrs794728626
geneviewrs794728626
scholarrs794728626
googlers794728626
pharmgkbrs794728626
gwascentralrs794728626
openSNPrs794728626
23andMers794728626
23andMe allrs794728626
SNP Nexus

SNPshotrs794728626
SNPdbers794728626
MSV3drs794728626
GWAS Ctlgrs794728626
Max Magnitude0
ClinVar
Risk rs794728626(A;A)
Alt rs794728626(A;A)
Reference rs794728626(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64574561C>T
CLNSRC
CLNACC RCV000182416.1,