rs1060499616

Orientation

minus

Stabilized

minus

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

Make rs1060499616(A;A)

Make rs1060499616(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

34880568

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs1060499616
dbSNP (classic)	rs1060499616
ClinGen	rs1060499616
ebi	rs1060499616
HLI	rs1060499616
Exac	rs1060499616
Gnomad	rs1060499616
Varsome	rs1060499616
LitVar	rs1060499616
Map	rs1060499616
PheGenI	rs1060499616
Biobank	rs1060499616
1000 genomes	rs1060499616
hgdp	rs1060499616
ensembl	rs1060499616
geneview	rs1060499616
scholar	rs1060499616
google	rs1060499616
pharmgkb	rs1060499616
gwascentral	rs1060499616
openSNP	rs1060499616
23andMe	rs1060499616
SNPshot	rs1060499616
SNPdbe	rs1060499616
MSV3d	rs1060499616
GWAS Ctlg	rs1060499616

Max Magnitude

0

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,