rs13306487

Orientation

plus

Stabilized

plus

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

Make rs13306487(A;A)

Make rs13306487(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

47292422

Gene

ITGB3

is a	snp
is	mentioned by
dbSNP	rs13306487
dbSNP (classic)	rs13306487
ClinGen	rs13306487
ebi	rs13306487
HLI	rs13306487
Exac	rs13306487
Gnomad	rs13306487
Varsome	rs13306487
LitVar	rs13306487
Map	rs13306487
PheGenI	rs13306487
Biobank	rs13306487
1000 genomes	rs13306487
hgdp	rs13306487
ensembl	rs13306487
geneview	rs13306487
scholar	rs13306487
google	rs13306487
pharmgkb	rs13306487
gwascentral	rs13306487
openSNP	rs13306487
23andMe	rs13306487
SNPshot	rs13306487
SNPdbe	rs13306487
MSV3d	rs13306487
GWAS Ctlg	rs13306487

GMAF

0.006887

Max Magnitude

0

OMIM	173470
Desc	Ca/Tu ALLOANTIGEN POLYMORPHISM
Variant	0009
Related	also

ClinVar
Risk	rs13306487(A;A) rs13306487(C;C) rs13306487(T;T)
Alt	rs13306487(A;A) rs13306487(C;C) rs13306487(T;T)
Reference	Rs13306487(G;G)
Significance	Pathogenic
Disease	Ca/Tu ALLOANTIGEN POLYMORPHISM Thrombocytopenia
Variation	info
Gene	ITGB3
CLNDBN	Ca/Tu ALLOANTIGEN POLYMORPHISM Thrombocytopenia, neonatal alloimmune
Reversed	0
HGVS	NC_000017.10:g.45369788G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014528.2, RCV000014529.19,