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rs794728630

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728630(A;T)
Make rs794728630(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804618
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728630
ebirs794728630
HLIrs794728630
Exacrs794728630
Varsomers794728630
Maprs794728630
PheGenIrs794728630
hapmaprs794728630
1000 genomesrs794728630
hgdprs794728630
ensemblrs794728630
gopubmedrs794728630
geneviewrs794728630
scholarrs794728630
googlers794728630
pharmgkbrs794728630
gwascentralrs794728630
openSNPrs794728630
23andMers794728630
23andMe allrs794728630
SNP Nexus

SNPshotrs794728630
SNPdbers794728630
MSV3drs794728630
GWAS Ctlgrs794728630
Max Magnitude0
ClinVar
Risk rs794728630(T;T)
Alt rs794728630(T;T)
Reference rs794728630(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572090T>A
CLNSRC
CLNACC RCV000182422.1,