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rs121913503

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913503(A;A)
Make rs121913503(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position90088606
GeneIDH2
is asnp
is mentioned by
dbSNPrs121913503
dbSNP (classic)rs121913503
ClinGenrs121913503
ebirs121913503
HLIrs121913503
Exacrs121913503
Gnomadrs121913503
Varsomers121913503
LitVarrs121913503
Maprs121913503
PheGenIrs121913503
Biobankrs121913503
1000 genomesrs121913503
hgdprs121913503
ensemblrs121913503
geneviewrs121913503
scholarrs121913503
googlers121913503
pharmgkbrs121913503
gwascentralrs121913503
openSNPrs121913503
23andMers121913503
23andMe allrs121913503
SNPshotrs121913503
SNPdbers121913503
MSV3drs121913503
GWAS Ctlgrs121913503
Max Magnitude0
ClinVar
Risk rs121913503(A;A) rs121913503(T;T)
Alt rs121913503(A;A) rs121913503(T;T)
Reference Rs121913503(G;G)
Significance Pathogenic
Disease Hepatocellular carcinoma Acute myeloid leukemia Colorectal Neoplasms Neoplasm of brain Brainstem glioma Myelodysplastic syndrome
Variation info
Gene IDH2
CLNDBN Hepatocellular carcinoma Acute myeloid leukemia Colorectal Neoplasms Neoplasm of brain Brainstem glioma Myelodysplastic syndrome
Reversed 1
HGVS NC_000015.9:g.90631838C>A; NC_000015.9:g.90631838C>T
CLNSRC
CLNACC RCV000422933.1, RCV000431159.1, RCV000433618.1, RCV000440163.1, RCV000440790.1, RCV000421863.1, RCV000426009.1, RCV000431485.1, RCV000432566.1, RCV000444071.1, RCV000445068.1,