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rs794728643

From SNPedia

Orientationminus
Make rs794728643(-;-)
Make rs794728643(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805043
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728643
ebirs794728643
HLIrs794728643
Exacrs794728643
Varsomers794728643
Maprs794728643
PheGenIrs794728643
hapmaprs794728643
1000 genomesrs794728643
hgdprs794728643
ensemblrs794728643
gopubmedrs794728643
geneviewrs794728643
scholarrs794728643
googlers794728643
pharmgkbrs794728643
gwascentralrs794728643
openSNPrs794728643
23andMers794728643
23andMe allrs794728643
SNP Nexus

SNPshotrs794728643
SNPdbers794728643
MSV3drs794728643
GWAS Ctlgrs794728643
Max Magnitude
ClinVar
Risk rs794728643(;)
Alt rs794728643(;)
Reference rs794728643(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572515delA
CLNSRC
CLNACC RCV000182440.1,