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rs794728650

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728650(A;A)
Make rs794728650(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807997
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728650
ebirs794728650
HLIrs794728650
Exacrs794728650
Varsomers794728650
Maprs794728650
PheGenIrs794728650
hapmaprs794728650
1000 genomesrs794728650
hgdprs794728650
ensemblrs794728650
gopubmedrs794728650
geneviewrs794728650
scholarrs794728650
googlers794728650
pharmgkbrs794728650
gwascentralrs794728650
openSNPrs794728650
23andMers794728650
23andMe allrs794728650
SNP Nexus

SNPshotrs794728650
SNPdbers794728650
MSV3drs794728650
GWAS Ctlgrs794728650
Max Magnitude0
ClinVar
Risk rs794728650(A;A)
Alt rs794728650(A;A)
Reference rs794728650(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575469C>T
CLNSRC
CLNACC RCV000182449.1,