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rs1057519749

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519749(G;T)
Make rs1057519749(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position34880579
GeneLOC102724584, RUNX1
is asnp
is mentioned by
dbSNPrs1057519749
dbSNP (old)rs1057519749
ClinGenrs1057519749
ebirs1057519749
HLIrs1057519749
Exacrs1057519749
Gnomadrs1057519749
Varsomers1057519749
Maprs1057519749
PheGenIrs1057519749
Biobankrs1057519749
1000 genomesrs1057519749
hgdprs1057519749
ensemblrs1057519749
gopubmedrs1057519749
geneviewrs1057519749
scholarrs1057519749
googlers1057519749
pharmgkbrs1057519749
gwascentralrs1057519749
openSNPrs1057519749
23andMers1057519749
23andMe allrs1057519749
SNPshotrs1057519749
SNPdbers1057519749
MSV3drs1057519749
GWAS Ctlgrs1057519749
Max Magnitude0
ClinVar
Risk rs1057519749(C;C) rs1057519749(T;T)
Alt rs1057519749(C;C) rs1057519749(T;T)
Reference Rs1057519749(G;G)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene RUNX1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000021.8:g.36252876C>A; NC_000021.8:g.36252876C>G
CLNSRC
CLNACC RCV000433391.1, RCV000441948.1,