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rs77963874

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs77963874(G;G)
Make rs77963874(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position47284512
GeneITGB3
is asnp
is mentioned by
dbSNPrs77963874
ebirs77963874
HLIrs77963874
Exacrs77963874
Varsomers77963874
Maprs77963874
PheGenIrs77963874
hapmaprs77963874
1000 genomesrs77963874
hgdprs77963874
ensemblrs77963874
gopubmedrs77963874
geneviewrs77963874
scholarrs77963874
googlers77963874
pharmgkbrs77963874
gwascentralrs77963874
openSNPrs77963874
23andMers77963874
23andMe allrs77963874
SNP Nexus

SNPshotrs77963874
SNPdbers77963874
MSV3drs77963874
GWAS Ctlgrs77963874
Max Magnitude0
ClinVar
Risk rs77963874(G;G)
Alt rs77963874(G;G)
Reference rs77963874(T;T)
Significance Pathogenic
Disease Glanzmann's thrombasthenia
Variation info
Gene ITGB3
CLNDBN Glanzmann's thrombasthenia
Reversed 0
HGVS NC_000017.10:g.45361878T>G
CLNSRC
CLNACC