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rs794728648

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728648(G;T)
Make rs794728648(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64808078
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728648
ebirs794728648
HLIrs794728648
Exacrs794728648
Varsomers794728648
Maprs794728648
PheGenIrs794728648
hapmaprs794728648
1000 genomesrs794728648
hgdprs794728648
ensemblrs794728648
gopubmedrs794728648
geneviewrs794728648
scholarrs794728648
googlers794728648
pharmgkbrs794728648
gwascentralrs794728648
openSNPrs794728648
23andMers794728648
23andMe allrs794728648
SNP Nexus

SNPshotrs794728648
SNPdbers794728648
MSV3drs794728648
GWAS Ctlgrs794728648
Max Magnitude0
ClinVar
Risk rs794728648(T;T)
Alt rs794728648(T;T)
Reference rs794728648(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575550C>A
CLNSRC
CLNACC RCV000182447.1,