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rs1057518837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518837(C;T)
Make rs1057518837(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position47299316
GeneITGB3
is asnp
is mentioned by
dbSNPrs1057518837
dbSNP (classic)rs1057518837
ClinGenrs1057518837
ebirs1057518837
HLIrs1057518837
Exacrs1057518837
Gnomadrs1057518837
Varsomers1057518837
LitVarrs1057518837
Maprs1057518837
PheGenIrs1057518837
Biobankrs1057518837
1000 genomesrs1057518837
hgdprs1057518837
ensemblrs1057518837
geneviewrs1057518837
scholarrs1057518837
googlers1057518837
pharmgkbrs1057518837
gwascentralrs1057518837
openSNPrs1057518837
23andMers1057518837
SNPshotrs1057518837
SNPdbers1057518837
MSV3drs1057518837
GWAS Ctlgrs1057518837
Max Magnitude0
ClinVar
Risk rs1057518837(T;T)
Alt rs1057518837(T;T)
Reference Rs1057518837(C;C)
Significance Probable-Pathogenic
Disease Abnormal bleeding Prolonged bleeding time
Variation info
Gene ITGB3
CLNDBN Abnormal bleeding Prolonged bleeding time
Reversed 0
HGVS NC_000017.10:g.45376682C>T
CLNSRC
CLNACC RCV000414924.1,