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rs587776810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776810(-;-)
Make rs587776810(-;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position34880554
GeneLOC101928240, RUNX1
is asnp
is mentioned by
dbSNPrs587776810
ebirs587776810
HLIrs587776810
Exacrs587776810
Varsomers587776810
Maprs587776810
PheGenIrs587776810
hapmaprs587776810
1000 genomesrs587776810
hgdprs587776810
ensemblrs587776810
gopubmedrs587776810
geneviewrs587776810
scholarrs587776810
googlers587776810
pharmgkbrs587776810
gwascentralrs587776810
openSNPrs587776810
23andMers587776810
23andMe allrs587776810
SNP Nexus

SNPshotrs587776810
SNPdbers587776810
MSV3drs587776810
GWAS Ctlgrs587776810
Max Magnitude0
ClinVar
Risk rs587776810(;)
Alt rs587776810(;)
Reference rs587776810(T;T)
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.36252851delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000015552.23,