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rs587776809

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776809(A;A)
Make rs587776809(A;C)
ReferenceGRCh38 38.1/142
Chromosome21
Position34880714
GeneLOC101928240, RUNX1
is asnp
is mentioned by
dbSNPrs587776809
ebirs587776809
HLIrs587776809
Exacrs587776809
Varsomers587776809
Maprs587776809
PheGenIrs587776809
hapmaprs587776809
1000 genomesrs587776809
hgdprs587776809
ensemblrs587776809
gopubmedrs587776809
geneviewrs587776809
scholarrs587776809
googlers587776809
pharmgkbrs587776809
gwascentralrs587776809
openSNPrs587776809
23andMers587776809
23andMe allrs587776809
SNP Nexus

SNPshotrs587776809
SNPdbers587776809
MSV3drs587776809
GWAS Ctlgrs587776809
Max Magnitude0
ClinVar
Risk rs587776809(A;A)
Alt rs587776809(A;A)
Reference rs587776809(C;C)
Significance Pathogenic
Disease Familial platelet disorder with associated myeloid malignancy
Variation info
Gene RUNX1
CLNDBN Familial platelet disorder with associated myeloid malignancy
Reversed 0
HGVS NC_000021.8:g.36253011C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015549.26,