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rs794728614

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728614(C;T)
Make rs794728614(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64810075
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728614
ebirs794728614
HLIrs794728614
Exacrs794728614
Varsomers794728614
Maprs794728614
PheGenIrs794728614
hapmaprs794728614
1000 genomesrs794728614
hgdprs794728614
ensemblrs794728614
gopubmedrs794728614
geneviewrs794728614
scholarrs794728614
googlers794728614
pharmgkbrs794728614
gwascentralrs794728614
openSNPrs794728614
23andMers794728614
23andMe allrs794728614
SNP Nexus

SNPshotrs794728614
SNPdbers794728614
MSV3drs794728614
GWAS Ctlgrs794728614
Max Magnitude0
ClinVar
Risk rs794728614(T;T)
Alt rs794728614(T;T)
Reference rs794728614(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64577547G>A
CLNSRC
CLNACC RCV000182401.1,