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rs11178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11178(C;C)
Make rs11178(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position101137803
GeneSERPINE1
is asnp
is mentioned by
dbSNPrs11178
dbSNP (classic)rs11178
ClinGenrs11178
ebirs11178
HLIrs11178
Exacrs11178
Gnomadrs11178
Varsomers11178
LitVarrs11178
Maprs11178
PheGenIrs11178
Biobankrs11178
1000 genomesrs11178
hgdprs11178
ensemblrs11178
geneviewrs11178
scholarrs11178
googlers11178
pharmgkbrs11178
gwascentralrs11178
openSNPrs11178
23andMers11178
SNPshotrs11178
SNPdbers11178
MSV3drs11178
GWAS Ctlgrs11178
GMAF0.4362
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 21752301OA-icon.png] Significant associations of PAI-1 genetic polymorphisms with osteonecrosis of the femoral head


[PMID 17761618OA-icon.png] 4G/5G plasminogen activator inhibitor-1 polymorphisms and haplotypes are associated with pneumonia.


[PMID 24135164OA-icon.png] Genetic polymorphisms in plasminogen activator inhibitor-1 predict susceptibility to steroid-induced osteonecrosis of the femoral head in Chinese population


ClinVar
Risk rs11178(C;C)
Alt rs11178(C;C)
Reference Rs11178(T;T)
Significance Non-pathogenic
Disease Plasminogen activator inhibitor type 1 deficiency
Variation info
Gene SERPINE1
CLNDBN Plasminogen activator inhibitor type 1 deficiency
Reversed 0
HGVS NC_000007.13:g.100781084T>C
CLNSRC
CLNACC RCV000341849.1,