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rs794728624

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728624(A;A)
Make rs794728624(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807613
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728624
ebirs794728624
HLIrs794728624
Exacrs794728624
Varsomers794728624
Maprs794728624
PheGenIrs794728624
hapmaprs794728624
1000 genomesrs794728624
hgdprs794728624
ensemblrs794728624
gopubmedrs794728624
geneviewrs794728624
scholarrs794728624
googlers794728624
pharmgkbrs794728624
gwascentralrs794728624
openSNPrs794728624
23andMers794728624
23andMe allrs794728624
SNP Nexus

SNPshotrs794728624
SNPdbers794728624
MSV3drs794728624
GWAS Ctlgrs794728624
Max Magnitude0
ClinVar
Risk rs794728624(A;A)
Alt rs794728624(A;A)
Reference rs794728624(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575085C>T
CLNSRC
CLNACC RCV000182413.1,