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rs1057519748

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519748(C;T)
Make rs1057519748(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position34859486
GeneLOC102724584, RUNX1
is asnp
is mentioned by
dbSNPrs1057519748
dbSNP (old)rs1057519748
ClinGenrs1057519748
ebirs1057519748
HLIrs1057519748
Exacrs1057519748
Gnomadrs1057519748
Varsomers1057519748
Maprs1057519748
PheGenIrs1057519748
Biobankrs1057519748
1000 genomesrs1057519748
hgdprs1057519748
ensemblrs1057519748
gopubmedrs1057519748
geneviewrs1057519748
scholarrs1057519748
googlers1057519748
pharmgkbrs1057519748
gwascentralrs1057519748
openSNPrs1057519748
23andMers1057519748
23andMe allrs1057519748
SNPshotrs1057519748
SNPdbers1057519748
MSV3drs1057519748
GWAS Ctlgrs1057519748
Max Magnitude0
ClinVar
Risk rs1057519748(T;T)
Alt rs1057519748(T;T)
Reference Rs1057519748(C;C)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene RUNX1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000021.8:g.36231783G>A
CLNSRC
CLNACC RCV000422235.1,