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rs794728654

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728654(C;T)
Make rs794728654(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805060
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728654
ebirs794728654
HLIrs794728654
Exacrs794728654
Varsomers794728654
Maprs794728654
PheGenIrs794728654
hapmaprs794728654
1000 genomesrs794728654
hgdprs794728654
ensemblrs794728654
gopubmedrs794728654
geneviewrs794728654
scholarrs794728654
googlers794728654
pharmgkbrs794728654
gwascentralrs794728654
openSNPrs794728654
23andMers794728654
23andMe allrs794728654
SNP Nexus

SNPshotrs794728654
SNPdbers794728654
MSV3drs794728654
GWAS Ctlgrs794728654
Max Magnitude0
ClinVar
Risk rs794728654(T;T)
Alt rs794728654(T;T)
Reference rs794728654(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572532G>A
CLNSRC
CLNACC RCV000182456.2,