rs766503255

Orientation

plus

Stabilized

plus

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

Make rs766503255(G;T)

Make rs766503255(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

44372408

Gene

ITGA2B

is a	snp
is	mentioned by
dbSNP	rs766503255
dbSNP (classic)	rs766503255
ClinGen	rs766503255
ebi	rs766503255
HLI	rs766503255
Exac	rs766503255
Gnomad	rs766503255
Varsome	rs766503255
LitVar	rs766503255
Map	rs766503255
PheGenI	rs766503255
Biobank	rs766503255
1000 genomes	rs766503255
hgdp	rs766503255
ensembl	rs766503255
geneview	rs766503255
scholar	rs766503255
google	rs766503255
pharmgkb	rs766503255
gwascentral	rs766503255
openSNP	rs766503255
23andMe	rs766503255
SNPshot	rs766503255
SNPdbe	rs766503255
MSV3d	rs766503255
GWAS Ctlg	rs766503255

Max Magnitude

0

ClinVar
Risk	rs766503255(A;A) rs766503255(T;T)
Alt	rs766503255(A;A) rs766503255(T;T)
Reference	Rs766503255(G;G)
Significance	Pathogenic
Disease	Platelet-type bleeding disorder 16
Variation	info
Gene	ITGA2B
CLNDBN	Platelet-type bleeding disorder 16
Reversed	0
HGVS	NC_000017.10:g.42449776G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043486.4,