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rs1057519750

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519750(A;A)
Make rs1057519750(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position34880580
GeneLOC102724584, RUNX1
is asnp
is mentioned by
dbSNPrs1057519750
dbSNP (old)rs1057519750
ClinGenrs1057519750
ebirs1057519750
HLIrs1057519750
Exacrs1057519750
Gnomadrs1057519750
Varsomers1057519750
Maprs1057519750
PheGenIrs1057519750
Biobankrs1057519750
1000 genomesrs1057519750
hgdprs1057519750
ensemblrs1057519750
gopubmedrs1057519750
geneviewrs1057519750
scholarrs1057519750
googlers1057519750
pharmgkbrs1057519750
gwascentralrs1057519750
openSNPrs1057519750
23andMers1057519750
23andMe allrs1057519750
SNPshotrs1057519750
SNPdbers1057519750
MSV3drs1057519750
GWAS Ctlgrs1057519750
Max Magnitude0
ClinVar
Risk rs1057519750(A;A)
Alt rs1057519750(A;A)
Reference Rs1057519750(G;G)
Significance Probable-Pathogenic
Disease Acute myeloid leukemia
Variation info
Gene RUNX1
CLNDBN Acute myeloid leukemia
Reversed 1
HGVS NC_000021.8:g.36252877C>T
CLNSRC
CLNACC RCV000426735.1,