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rs794728659

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs794728659(-;GT)
Make rs794728659(GT;GT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position64804632
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs794728659
ClinGenrs794728659
ebirs794728659
HLIrs794728659
Exacrs794728659
Varsomers794728659
Maprs794728659
PheGenIrs794728659
hapmaprs794728659
1000 genomesrs794728659
hgdprs794728659
ensemblrs794728659
gopubmedrs794728659
geneviewrs794728659
scholarrs794728659
googlers794728659
pharmgkbrs794728659
gwascentralrs794728659
openSNPrs794728659
23andMers794728659
23andMe allrs794728659
SNP Nexus

SNPshotrs794728659
SNPdbers794728659
MSV3drs794728659
GWAS Ctlgrs794728659
Max Magnitude0
ClinVar
Risk rs794728659(GT;GT)
Alt rs794728659(GT;GT)
Reference Rs794728659(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572105_64572106dupAC
CLNSRC
CLNACC RCV000182462.1,