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rs794728649

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728649(C;C)
Make rs794728649(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64807998
GeneMEN1
is asnp
is mentioned by
dbSNPrs794728649
ebirs794728649
HLIrs794728649
Exacrs794728649
Varsomers794728649
Maprs794728649
PheGenIrs794728649
hapmaprs794728649
1000 genomesrs794728649
hgdprs794728649
ensemblrs794728649
gopubmedrs794728649
geneviewrs794728649
scholarrs794728649
googlers794728649
pharmgkbrs794728649
gwascentralrs794728649
openSNPrs794728649
23andMers794728649
23andMe allrs794728649
SNP Nexus

SNPshotrs794728649
SNPdbers794728649
MSV3drs794728649
GWAS Ctlgrs794728649
Max Magnitude0
ClinVar
Risk rs794728649(C;C)
Alt rs794728649(C;C)
Reference rs794728649(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64575470A>G
CLNSRC
CLNACC RCV000182448.1,