rs3809865

plus

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

Make rs3809865(A;A)

Make rs3809865(A;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

47311220

Gene	ITGB3, THCAT158

is a	snp
is	mentioned by
dbSNP	rs3809865
dbSNP (classic)	rs3809865
ClinGen	rs3809865
ebi	rs3809865
HLI	rs3809865
Exac	rs3809865
Gnomad	rs3809865
Varsome	rs3809865
LitVar	rs3809865
Map	rs3809865
PheGenI	rs3809865
Biobank	rs3809865
1000 genomes	rs3809865
hgdp	rs3809865
ensembl	rs3809865
geneview	rs3809865
scholar	rs3809865
google	rs3809865
pharmgkb	rs3809865
gwascentral	rs3809865
openSNP	rs3809865
23andMe	rs3809865
SNPshot	rs3809865
SNPdbe	rs3809865
MSV3d	rs3809865
GWAS Ctlg	rs3809865

GMAF

0.2769

Max Magnitude

0

?

(A;A) (A;T) (T;T)

28

[PMID 22271436] Single-nucleotide polymorphisms of integrins are associated with the risk and lymph node metastasis of oral squamous cell carcinoma

[PMID 17999363 ] Multifactor dimensionality reduction-phenomics: a novel method to capture genetic heterogeneity with use of phenotypic variables.

[PMID 19588468 ] Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.

[PMID 20403199 ] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.

[PMID 23451109 ] Genetic variation of ITGB3 is associated with asthma in Chinese Han children

[PMID 24769516] Polymorphisms of microRNA-Binding Sites in Integrin Genes Are Associated with Oral Squamous Cell Carcinoma Susceptibility and Progression

ClinVar
Risk	rs3809865(A;A)
Alt	rs3809865(A;A)
Reference	Rs3809865(T;T)
Significance	Non-pathogenic
Disease	Glanzmann thrombasthenia
Variation	info
Gene	ITGB3 THCAT158
CLNDBN	Glanzmann thrombasthenia
Reversed	0
HGVS	NC_000017.10:g.45388586T>A
CLNSRC
CLNACC	RCV000370303.1,