rs17292650

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs17292650(G;T)

Make rs17292650(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

43338136

Gene

MPL

is a	snp
is	mentioned by
dbSNP	rs17292650
dbSNP (classic)	rs17292650
ClinGen	rs17292650
ebi	rs17292650
HLI	rs17292650
Exac	rs17292650
Gnomad	rs17292650
Varsome	rs17292650
LitVar	rs17292650
Map	rs17292650
PheGenI	rs17292650
Biobank	rs17292650
1000 genomes	rs17292650
hgdp	rs17292650
ensembl	rs17292650
geneview	rs17292650
scholar	rs17292650
google	rs17292650
pharmgkb	rs17292650
gwascentral	rs17292650
openSNP	rs17292650
23andMe	rs17292650
SNPshot	rs17292650
SNPdbe	rs17292650
MSV3d	rs17292650
GWAS Ctlg	rs17292650

GMAF

0.01148

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

OMIM	159530
Desc	THROMBOCYTOSIS, SUSCEPTIBILITY TO
Variant	0009
Related	also

ClinVar
Risk	rs17292650(T;T)
Alt	rs17292650(T;T)
Reference	Rs17292650(G;G)
Significance	Other
Disease	Thrombocytosis not specified Essential thrombocythemia Congenital amegakaryocytic thrombocytopenia
Variation	info
Gene	MPL
CLNDBN	Thrombocytosis, benign familial microcytic not specified Essential thrombocythemia Congenital amegakaryocytic thrombocytopenia
Reversed	0
HGVS	NC_000001.10:g.43803807G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000015225.3, RCV000121535.1, RCV000359577.1, RCV000400040.1,