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rs398124436

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398124436(-;-)
Make rs398124436(-;A)
Make rs398124436(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position64804481
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs398124436
ebirs398124436
HLIrs398124436
Exacrs398124436
Varsomers398124436
Maprs398124436
PheGenIrs398124436
hapmaprs398124436
1000 genomesrs398124436
hgdprs398124436
ensemblrs398124436
gopubmedrs398124436
geneviewrs398124436
scholarrs398124436
googlers398124436
pharmgkbrs398124436
gwascentralrs398124436
openSNPrs398124436
23andMers398124436
23andMe allrs398124436
SNP Nexus

SNPshotrs398124436
SNPdbers398124436
MSV3drs398124436
GWAS Ctlgrs398124436
Max Magnitude0
ClinVar
Risk rs398124436(A;A)
Alt rs398124436(A;A)
Reference rs398124436(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64571954dupT
CLNSRC ClinVar
CLNACC RCV000082335.3,