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rs794728645

From SNPedia

Orientationminus
Make rs794728645(-;-)
Make rs794728645(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804516
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728645
ebirs794728645
HLIrs794728645
Exacrs794728645
Varsomers794728645
Maprs794728645
PheGenIrs794728645
hapmaprs794728645
1000 genomesrs794728645
hgdprs794728645
ensemblrs794728645
gopubmedrs794728645
geneviewrs794728645
scholarrs794728645
googlers794728645
pharmgkbrs794728645
gwascentralrs794728645
openSNPrs794728645
23andMers794728645
23andMe allrs794728645
SNP Nexus

SNPshotrs794728645
SNPdbers794728645
MSV3drs794728645
GWAS Ctlgrs794728645
Max Magnitude
ClinVar
Risk rs794728645(;)
Alt rs794728645(;)
Reference rs794728645(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571988delG
CLNSRC
CLNACC RCV000182443.1,