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rs794728628

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728628(A;A)
Make rs794728628(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64805199
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728628
ebirs794728628
HLIrs794728628
Exacrs794728628
Varsomers794728628
Maprs794728628
PheGenIrs794728628
hapmaprs794728628
1000 genomesrs794728628
hgdprs794728628
ensemblrs794728628
gopubmedrs794728628
geneviewrs794728628
scholarrs794728628
googlers794728628
pharmgkbrs794728628
gwascentralrs794728628
openSNPrs794728628
23andMers794728628
23andMe allrs794728628
SNP Nexus

SNPshotrs794728628
SNPdbers794728628
MSV3drs794728628
GWAS Ctlgrs794728628
Max Magnitude0
ClinVar
Risk rs794728628(A;A)
Alt rs794728628(A;A)
Reference rs794728628(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572671C>T
CLNSRC
CLNACC RCV000182418.1,