rs587776809

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs587776809(A;A)

Make rs587776809(A;C)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34880714

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs587776809
dbSNP (classic)	rs587776809
ClinGen	rs587776809
ebi	rs587776809
HLI	rs587776809
Exac	rs587776809
Gnomad	rs587776809
Varsome	rs587776809
LitVar	rs587776809
Map	rs587776809
PheGenI	rs587776809
Biobank	rs587776809
1000 genomes	rs587776809
hgdp	rs587776809
ensembl	rs587776809
geneview	rs587776809
scholar	rs587776809
google	rs587776809
pharmgkb	rs587776809
gwascentral	rs587776809
openSNP	rs587776809
23andMe	rs587776809
SNPshot	rs587776809
SNPdbe	rs587776809
MSV3d	rs587776809
GWAS Ctlg	rs587776809

Max Magnitude

0

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,