Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519736

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519736(C;C)
Make rs1057519736(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position90088605
GeneIDH2
is asnp
is mentioned by
dbSNPrs1057519736
dbSNP (old)rs1057519736
ClinGenrs1057519736
ebirs1057519736
HLIrs1057519736
Exacrs1057519736
Gnomadrs1057519736
Varsomers1057519736
Maprs1057519736
PheGenIrs1057519736
Biobankrs1057519736
1000 genomesrs1057519736
hgdprs1057519736
ensemblrs1057519736
gopubmedrs1057519736
geneviewrs1057519736
scholarrs1057519736
googlers1057519736
pharmgkbrs1057519736
gwascentralrs1057519736
openSNPrs1057519736
23andMers1057519736
23andMe allrs1057519736
SNPshotrs1057519736
SNPdbers1057519736
MSV3drs1057519736
GWAS Ctlgrs1057519736
Max Magnitude0
ClinVar
Risk rs1057519736(C;C)
Alt rs1057519736(C;C)
Reference Rs1057519736(G;G)
Significance Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene IDH2
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000015.9:g.90631837C>G
CLNSRC
CLNACC RCV000420486.1,