rs587776810

Orientation

plus

Stabilized

plus

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

Make rs587776810(-;-)

Make rs587776810(-;T)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34880554

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs587776810
dbSNP (classic)	rs587776810
ClinGen	rs587776810
ebi	rs587776810
HLI	rs587776810
Exac	rs587776810
Gnomad	rs587776810
Varsome	rs587776810
LitVar	rs587776810
Map	rs587776810
PheGenI	rs587776810
Biobank	rs587776810
1000 genomes	rs587776810
hgdp	rs587776810
ensembl	rs587776810
geneview	rs587776810
scholar	rs587776810
google	rs587776810
pharmgkb	rs587776810
gwascentral	rs587776810
openSNP	rs587776810
23andMe	rs587776810
SNPshot	rs587776810
SNPdbe	rs587776810
MSV3d	rs587776810
GWAS Ctlg	rs587776810

Max Magnitude

0

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,