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rs1060499616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499616(A;A)
Make rs1060499616(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome21
Position34880568
GeneLOC102724584, RUNX1
is asnp
is mentioned by
dbSNPrs1060499616
dbSNP (classic)rs1060499616
ClinGenrs1060499616
ebirs1060499616
HLIrs1060499616
Exacrs1060499616
Gnomadrs1060499616
Varsomers1060499616
LitVarrs1060499616
Maprs1060499616
PheGenIrs1060499616
Biobankrs1060499616
1000 genomesrs1060499616
hgdprs1060499616
ensemblrs1060499616
geneviewrs1060499616
scholarrs1060499616
googlers1060499616
pharmgkbrs1060499616
gwascentralrs1060499616
openSNPrs1060499616
23andMers1060499616
23andMe allrs1060499616
SNPshotrs1060499616
SNPdbers1060499616
MSV3drs1060499616
GWAS Ctlgrs1060499616
Max Magnitude0
ClinVar
Risk rs1060499616(A;A)
Alt rs1060499616(A;A)
Reference Rs1060499616(G;G)
Significance Probable-Pathogenic
Disease Familial platelet disorder with associated myeloid malignancy
Variation info
Gene RUNX1
CLNDBN Familial platelet disorder with associated myeloid malignancy
Reversed 1
HGVS NC_000021.8:g.36252865C>T
CLNSRC
CLNACC RCV000477937.1,