rs11099592
Orientation | plus |
Stabilized | plus |
Make rs11099592(C;C) |
Make rs11099592(C;T) |
Make rs11099592(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 83309466 |
Gene | HPSE |
is a | snp |
is | mentioned by |
dbSNP | rs11099592 |
dbSNP (classic) | rs11099592 |
ClinGen | rs11099592 |
ebi | rs11099592 |
HLI | rs11099592 |
Exac | rs11099592 |
Gnomad | rs11099592 |
Varsome | rs11099592 |
LitVar | rs11099592 |
Map | rs11099592 |
PheGenI | rs11099592 |
Biobank | rs11099592 |
1000 genomes | rs11099592 |
hgdp | rs11099592 |
ensembl | rs11099592 |
geneview | rs11099592 |
scholar | rs11099592 |
rs11099592 | |
pharmgkb | rs11099592 |
gwascentral | rs11099592 |
openSNP | rs11099592 |
23andMe | rs11099592 |
SNPshot | rs11099592 |
SNPdbe | rs11099592 |
MSV3d | rs11099592 |
GWAS Ctlg | rs11099592 |
GMAF | 0.1919 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20578081] Association of heparanase gene (HPSE-1) single nucleotide polymorphisms with gastric cancer
[PMID 22276173] 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 19406828] Inverse correlation between HPSE gene single nucleotide polymorphisms and heparanase expression: possibility of multiple levels of heparanase regulation.
[PMID 29955035] Identification of strong intron enhancer in the heparanase gene: effect of functional rs4693608 variant on HPSE enhancer activity in hematological and solid malignancies.
- Is a snp
- In dbSNP
- SNPs on chromosome 4
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2c
- On chip Ancestry v2d