Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728634

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728634(C;C)
Make rs794728634(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804437
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728634
ebirs794728634
HLIrs794728634
Exacrs794728634
Varsomers794728634
Maprs794728634
PheGenIrs794728634
hapmaprs794728634
1000 genomesrs794728634
hgdprs794728634
ensemblrs794728634
gopubmedrs794728634
geneviewrs794728634
scholarrs794728634
googlers794728634
pharmgkbrs794728634
gwascentralrs794728634
openSNPrs794728634
23andMers794728634
23andMe allrs794728634
SNP Nexus

SNPshotrs794728634
SNPdbers794728634
MSV3drs794728634
GWAS Ctlgrs794728634
Max Magnitude0
ClinVar
Risk rs794728634(C;C)
Alt rs794728634(C;C)
Reference rs794728634(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571909A>G
CLNSRC
CLNACC RCV000182428.2,