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rs398124435

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124435(G;T)
Make rs398124435(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64805076
GeneMAP4K2, MEN1
is asnp
is mentioned by
dbSNPrs398124435
ebirs398124435
HLIrs398124435
Exacrs398124435
Varsomers398124435
Maprs398124435
PheGenIrs398124435
hapmaprs398124435
1000 genomesrs398124435
hgdprs398124435
ensemblrs398124435
gopubmedrs398124435
geneviewrs398124435
scholarrs398124435
googlers398124435
pharmgkbrs398124435
gwascentralrs398124435
openSNPrs398124435
23andMers398124435
23andMe allrs398124435
SNP Nexus

SNPshotrs398124435
SNPdbers398124435
MSV3drs398124435
GWAS Ctlgrs398124435
Max Magnitude0
ClinVar
Risk rs398124435(T;T)
Alt rs398124435(T;T)
Reference rs398124435(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MAP4K2 MEN1
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.64572548C>A
CLNSRC HGMD
CLNACC RCV000082333.5,