rs74664206

Orientation

minus

Stabilized

minus

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

Make rs74664206(C;C)

Make rs74664206(C;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

44374352

Gene

ITGA2B

is a	snp
is	mentioned by
dbSNP	rs74664206
dbSNP (classic)	rs74664206
ClinGen	rs74664206
ebi	rs74664206
HLI	rs74664206
Exac	rs74664206
Gnomad	rs74664206
Varsome	rs74664206
LitVar	rs74664206
Map	rs74664206
PheGenI	rs74664206
Biobank	rs74664206
1000 genomes	rs74664206
hgdp	rs74664206
ensembl	rs74664206
geneview	rs74664206
scholar	rs74664206
google	rs74664206
pharmgkb	rs74664206
gwascentral	rs74664206
openSNP	rs74664206
23andMe	rs74664206
SNPshot	rs74664206
SNPdbe	rs74664206
MSV3d	rs74664206
GWAS Ctlg	rs74664206

Max Magnitude

0

ClinVar
Risk	rs74664206(C;C)
Alt	rs74664206(C;C)
Reference	Rs74664206(T;T)
Significance	Pathogenic
Disease	Glanzmann's thrombasthenia
Variation	info
Gene	ITGA2B
CLNDBN	Glanzmann's thrombasthenia
Reversed	1
HGVS	NC_000017.10:g.42451720A>G
CLNSRC
CLNACC

[PMID 9215749] Hematologically important mutations: Glanzmann thrombasthenia.