rs797045927

Orientation

minus

Stabilized

minus

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

Make rs797045927(A;A)

Make rs797045927(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

21

Position

34859530

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs797045927
dbSNP (classic)	rs797045927
ClinGen	rs797045927
ebi	rs797045927
HLI	rs797045927
Exac	rs797045927
Gnomad	rs797045927
Varsome	rs797045927
LitVar	rs797045927
Map	rs797045927
PheGenI	rs797045927
Biobank	rs797045927
1000 genomes	rs797045927
hgdp	rs797045927
ensembl	rs797045927
geneview	rs797045927
scholar	rs797045927
google	rs797045927
pharmgkb	rs797045927
gwascentral	rs797045927
openSNP	rs797045927
23andMe	rs797045927
SNPshot	rs797045927
SNPdbe	rs797045927
MSV3d	rs797045927
GWAS Ctlg	rs797045927

Max Magnitude

0

ClinVar
Risk	rs797045927(A;A)
Alt	rs797045927(A;A)
Reference	Rs797045927(T;T)
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.36231827A>T
CLNSRC
CLNACC	RCV000192486.1,