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rs794728632

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728632(G;T)
Make rs794728632(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804480
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728632
ebirs794728632
HLIrs794728632
Exacrs794728632
Varsomers794728632
Maprs794728632
PheGenIrs794728632
hapmaprs794728632
1000 genomesrs794728632
hgdprs794728632
ensemblrs794728632
gopubmedrs794728632
geneviewrs794728632
scholarrs794728632
googlers794728632
pharmgkbrs794728632
gwascentralrs794728632
openSNPrs794728632
23andMers794728632
23andMe allrs794728632
SNP Nexus

SNPshotrs794728632
SNPdbers794728632
MSV3drs794728632
GWAS Ctlgrs794728632
Max Magnitude0
ClinVar
Risk rs794728632(T;T)
Alt rs794728632(T;T)
Reference rs794728632(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571952C>A
CLNSRC
CLNACC RCV000182426.1,