rs398122374

Orientation

plus

Stabilized

plus

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

Make rs398122374(C;C)

Make rs398122374(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

47307567

Gene	ITGB3, THCAT158

is a	snp
is	mentioned by
dbSNP	rs398122374
dbSNP (classic)	rs398122374
ClinGen	rs398122374
ebi	rs398122374
HLI	rs398122374
Exac	rs398122374
Gnomad	rs398122374
Varsome	rs398122374
LitVar	rs398122374
Map	rs398122374
PheGenI	rs398122374
Biobank	rs398122374
1000 genomes	rs398122374
hgdp	rs398122374
ensembl	rs398122374
geneview	rs398122374
scholar	rs398122374
google	rs398122374
pharmgkb	rs398122374
gwascentral	rs398122374
openSNP	rs398122374
23andMe	rs398122374
SNPshot	rs398122374
SNPdbe	rs398122374
MSV3d	rs398122374
GWAS Ctlg	rs398122374

Max Magnitude

0

ClinVar
Risk	rs398122374(C;C)
Alt	rs398122374(C;C)
Reference	Rs398122374(T;T)
Significance	Pathogenic
Disease	Platelet-type bleeding disorder 16
Variation	info
Gene	ITGB3 THCAT158
CLNDBN	Platelet-type bleeding disorder 16
Reversed	0
HGVS	NC_000017.10:g.45384933T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043482.25,