rs267607026

Orientation

minus

Stabilized

minus

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

Make rs267607026(A;A)

Make rs267607026(A;C)

Reference

GRCh38 38.1/141

Chromosome

21

Position

34880598

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs267607026
dbSNP (classic)	rs267607026
ClinGen	rs267607026
ebi	rs267607026
HLI	rs267607026
Exac	rs267607026
Gnomad	rs267607026
Varsome	rs267607026
LitVar	rs267607026
Map	rs267607026
PheGenI	rs267607026
Biobank	rs267607026
1000 genomes	rs267607026
hgdp	rs267607026
ensembl	rs267607026
geneview	rs267607026
scholar	rs267607026
google	rs267607026
pharmgkb	rs267607026
gwascentral	rs267607026
openSNP	rs267607026
23andMe	rs267607026
SNPshot	rs267607026
SNPdbe	rs267607026
MSV3d	rs267607026
GWAS Ctlg	rs267607026

Max Magnitude

0

ClinVar
Risk	rs267607026(A;A)
Alt	rs267607026(A;A)
Reference	Rs267607026(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	1
HGVS	NC_000021.8:g.36252895G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015558.26,