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rs4634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4634(A;A)
Make rs4634(A;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position47292423
GeneITGB3
is asnp
is mentioned by
dbSNPrs4634
dbSNP (old)rs4634
ClinGenrs4634
ebirs4634
HLIrs4634
Exacrs4634
Gnomadrs4634
Varsomers4634
Maprs4634
PheGenIrs4634
Biobankrs4634
1000 genomesrs4634
hgdprs4634
ensemblrs4634
gopubmedrs4634
geneviewrs4634
scholarrs4634
googlers4634
pharmgkbrs4634
gwascentralrs4634
openSNPrs4634
23andMers4634
23andMe allrs4634
SNP Nexus

SNPshotrs4634
SNPdbers4634
MSV3drs4634
GWAS Ctlgrs4634
GMAF0.2948
Max Magnitude0

[PMID 22246292] Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases

ClinVar
Risk rs4634(A;A)
Alt rs4634(A;A)
Reference Rs4634(G;G)
Significance Non-pathogenic
Disease not specified Glanzmann thrombasthenia
Variation info
Gene ITGB3
CLNDBN not specified Glanzmann thrombasthenia
Reversed 0
HGVS NC_000017.10:g.45369789G>A
CLNSRC
CLNACC RCV000241947.1, RCV000394843.1,