rs76066357

Orientation

plus

Stabilized

plus

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

Make rs76066357(C;C)

Make rs76066357(C;G)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

44385686

Gene

ITGA2B

is a	snp
is	mentioned by
dbSNP	rs76066357
dbSNP (classic)	rs76066357
ClinGen	rs76066357
ebi	rs76066357
HLI	rs76066357
Exac	rs76066357
Gnomad	rs76066357
Varsome	rs76066357
LitVar	rs76066357
Map	rs76066357
PheGenI	rs76066357
Biobank	rs76066357
1000 genomes	rs76066357
hgdp	rs76066357
ensembl	rs76066357
geneview	rs76066357
scholar	rs76066357
google	rs76066357
pharmgkb	rs76066357
gwascentral	rs76066357
openSNP	rs76066357
23andMe	rs76066357
SNPshot	rs76066357
SNPdbe	rs76066357
MSV3d	rs76066357
GWAS Ctlg	rs76066357

Max Magnitude

0

ClinVar
Risk	rs76066357(C;C)
Alt	rs76066357(C;C)
Reference	Rs76066357(G;G)
Significance	Pathogenic
Disease	Glanzmann thrombasthenia not specified
Variation	info
Gene	ITGA2B
CLNDBN	Glanzmann thrombasthenia not specified
Reversed	0
HGVS	NC_000017.10:g.42463054G>C
CLNSRC
CLNACC	RCV000198077.1, RCV000244527.1,