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rs11099592

From SNPedia

Orientationplus
Stabilizedplus
Make rs11099592(C;C)
Make rs11099592(C;T)
Make rs11099592(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position83309466
GeneHPSE
is asnp
is mentioned by
dbSNPrs11099592
dbSNP (classic)rs11099592
ClinGenrs11099592
ebirs11099592
HLIrs11099592
Exacrs11099592
Gnomadrs11099592
Varsomers11099592
LitVarrs11099592
Maprs11099592
PheGenIrs11099592
Biobankrs11099592
1000 genomesrs11099592
hgdprs11099592
ensemblrs11099592
geneviewrs11099592
scholarrs11099592
googlers11099592
pharmgkbrs11099592
gwascentralrs11099592
openSNPrs11099592
23andMers11099592
SNPshotrs11099592
SNPdbers11099592
MSV3drs11099592
GWAS Ctlgrs11099592
GMAF0.1919
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 20578081] Association of heparanase gene (HPSE-1) single nucleotide polymorphisms with gastric cancer


[PMID 22276173OA-icon.png] Polymorphisms and a haplotype in heparanase gene associations with the progression and prognosis of gastric cancer in a northern chinese population


[PMID 17611567] Association of heparanase gene (HPSE) single nucleotide polymorphisms with hematological malignancies.


[PMID 19406828OA-icon.png] Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation.


[PMID 29955035OA-icon.png] Identification of strong intron enhancer in the heparanase gene: effect of functional rs4693608 variant on HPSE enhancer activity in hematological and solid malignancies.