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rs1057519906

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519906(A;T)
Make rs1057519906(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position90088607
GeneIDH2
is asnp
is mentioned by
dbSNPrs1057519906
dbSNP (old)rs1057519906
ClinGenrs1057519906
ebirs1057519906
HLIrs1057519906
Exacrs1057519906
Gnomadrs1057519906
Varsomers1057519906
LitVarrs1057519906
Maprs1057519906
PheGenIrs1057519906
Biobankrs1057519906
1000 genomesrs1057519906
hgdprs1057519906
ensemblrs1057519906
gopubmedrs1057519906
geneviewrs1057519906
scholarrs1057519906
googlers1057519906
pharmgkbrs1057519906
gwascentralrs1057519906
openSNPrs1057519906
23andMers1057519906
23andMe allrs1057519906
SNPshotrs1057519906
SNPdbers1057519906
MSV3drs1057519906
GWAS Ctlgrs1057519906
Max Magnitude0
ClinVar
Risk rs1057519906(G;G) rs1057519906(T;T)
Alt rs1057519906(G;G) rs1057519906(T;T)
Reference Rs1057519906(A;A)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms Neoplasm of brain Brainstem glioma Acute myeloid leukemia Hepatocellular carcinoma
Variation info
Gene IDH2
CLNDBN Colorectal Neoplasms Neoplasm of brain Brainstem glioma Acute myeloid leukemia Hepatocellular carcinoma
Reversed 1
HGVS NC_000015.9:g.90631839T>A; NC_000015.9:g.90631839T>C
CLNSRC
CLNACC RCV000420203.1, RCV000425002.1, RCV000431322.1, RCV000437853.1, RCV000444821.1, RCV000419393.1, RCV000423117.1, RCV000429662.1, RCV000438062.1, RCV000440787.1,