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rs794728615

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728615(C;T)
Make rs794728615(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64810025
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728615
ebirs794728615
HLIrs794728615
Exacrs794728615
Varsomers794728615
Maprs794728615
PheGenIrs794728615
hapmaprs794728615
1000 genomesrs794728615
hgdprs794728615
ensemblrs794728615
gopubmedrs794728615
geneviewrs794728615
scholarrs794728615
googlers794728615
pharmgkbrs794728615
gwascentralrs794728615
openSNPrs794728615
23andMers794728615
23andMe allrs794728615
SNP Nexus

SNPshotrs794728615
SNPdbers794728615
MSV3drs794728615
GWAS Ctlgrs794728615
Max Magnitude0
ClinVar
Risk rs794728615(T;T)
Alt rs794728615(T;T)
Reference rs794728615(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577497G>A
CLNSRC
CLNACC RCV000182403.1,