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rs76066357

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs76066357(C;C)
Make rs76066357(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position44385686
GeneITGA2B
is asnp
is mentioned by
dbSNPrs76066357
ebirs76066357
HLIrs76066357
Exacrs76066357
Varsomers76066357
Maprs76066357
PheGenIrs76066357
hapmaprs76066357
1000 genomesrs76066357
hgdprs76066357
ensemblrs76066357
gopubmedrs76066357
geneviewrs76066357
scholarrs76066357
googlers76066357
pharmgkbrs76066357
gwascentralrs76066357
openSNPrs76066357
23andMers76066357
23andMe allrs76066357
SNP Nexus

SNPshotrs76066357
SNPdbers76066357
MSV3drs76066357
GWAS Ctlgrs76066357
Max Magnitude0
ClinVar
Risk rs76066357(C;C)
Alt rs76066357(C;C)
Reference rs76066357(G;G)
Significance Pathogenic
Disease Glanzmann's thrombasthenia
Variation info
Gene ITGA2B
CLNDBN Glanzmann's thrombasthenia
Reversed 0
HGVS NC_000017.10:g.42463054G>C
CLNSRC
CLNACC RCV000198077.1,