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rs267606870

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606870(C;G)
Make rs267606870(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position90088703
GeneIDH2
is asnp
is mentioned by
dbSNPrs267606870
ClinGenrs267606870
ebirs267606870
HLIrs267606870
Exacrs267606870
Varsomers267606870
Maprs267606870
PheGenIrs267606870
hapmaprs267606870
1000 genomesrs267606870
hgdprs267606870
ensemblrs267606870
gopubmedrs267606870
geneviewrs267606870
scholarrs267606870
googlers267606870
pharmgkbrs267606870
gwascentralrs267606870
openSNPrs267606870
23andMers267606870
23andMe allrs267606870
SNP Nexus

SNPshotrs267606870
SNPdbers267606870
MSV3drs267606870
GWAS Ctlgrs267606870
Max Magnitude0
ClinVar
Risk rs267606870(G;G) rs267606870(T;T)
Alt rs267606870(G;G) rs267606870(T;T)
Reference Rs267606870(C;C)
Significance Pathogenic
Disease Acute myeloid leukemia Colorectal Neoplasms Myelodysplastic syndrome Squamous cell carcinoma of the head and neck Multiple myeloma D-2-hydroxyglutaric aciduria 2
Variation info
Gene IDH2
CLNDBN Acute myeloid leukemia Colorectal Neoplasms Myelodysplastic syndrome Squamous cell carcinoma of the head and neck Multiple myeloma D-2-hydroxyglutaric aciduria 2
Reversed 1
HGVS NC_000015.9:g.90631935G>A; NC_000015.9:g.90631935G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000421344.1, RCV000422389.1, RCV000428106.1, RCV000438361.1, RCV000438997.1, RCV000015832.26,