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rs794728631

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728631(C;T)
Make rs794728631(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804507
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728631
ebirs794728631
HLIrs794728631
Exacrs794728631
Varsomers794728631
Maprs794728631
PheGenIrs794728631
hapmaprs794728631
1000 genomesrs794728631
hgdprs794728631
ensemblrs794728631
gopubmedrs794728631
geneviewrs794728631
scholarrs794728631
googlers794728631
pharmgkbrs794728631
gwascentralrs794728631
openSNPrs794728631
23andMers794728631
23andMe allrs794728631
SNP Nexus

SNPshotrs794728631
SNPdbers794728631
MSV3drs794728631
GWAS Ctlgrs794728631
Max Magnitude0
ClinVar
Risk rs794728631(T;T)
Alt rs794728631(T;T)
Reference rs794728631(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571979G>A
CLNSRC
CLNACC RCV000182425.2,