rs1050565
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | normal |
(A;G) | 0 | normal |
(G;G) | 2 | if testicular cancer patient, 5x poorer response to bleomycin chemotherapy |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 30249058 |
Gene | BLMH |
is a | snp |
is | mentioned by |
dbSNP | rs1050565 |
dbSNP (classic) | rs1050565 |
ClinGen | rs1050565 |
ebi | rs1050565 |
HLI | rs1050565 |
Exac | rs1050565 |
Gnomad | rs1050565 |
Varsome | rs1050565 |
LitVar | rs1050565 |
Map | rs1050565 |
PheGenI | rs1050565 |
Biobank | rs1050565 |
1000 genomes | rs1050565 |
hgdp | rs1050565 |
ensembl | rs1050565 |
geneview | rs1050565 |
scholar | rs1050565 |
rs1050565 | |
pharmgkb | rs1050565 |
gwascentral | rs1050565 |
openSNP | rs1050565 |
23andMe | rs1050565 |
SNPshot | rs1050565 |
SNPdbe | rs1050565 |
MSV3d | rs1050565 |
GWAS Ctlg | rs1050565 |
GMAF | 0.2736 |
Max Magnitude | 2 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Testicular cancer patients may be treated with bleomycin, a cytotoxic drug that is essential component of chemotherapy regimens for this cancer, officially known as disseminated testicular germ-cell cancer (TC). rs1050565 is a SNP in the BLMH gene. This gene encodes a protein that can inactivate bleomycin.
Based on a study of 300 TC patients treated with bleomycin, a testicular cancer patient with a rs1050565(G;G) genotype has an odds ratio of 4.97 (CI: 2.17 - 11.39) for TC-related death compared to (A;G) or (A;A) genotypes. The rs1050565(G;G) genotype also shows a higher prevalence of early relapses.[PMID 18398146]
ClinVar | |
---|---|
Risk | Rs1050565(G;G) |
Alt | Rs1050565(G;G) |
Reference | Rs1050565(A;A) |
Significance | Non-pathogenic |
Disease | BLEOMYCIN HYDROLASE POLYMORPHISM |
Variation | info |
Gene | BLMH |
CLNDBN | BLEOMYCIN HYDROLASE POLYMORPHISM |
Reversed | 1 |
HGVS | NC_000017.10:g.28576076T>C |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000007670.2, |
[PMID 15995945] Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.
[PMID 19673036] Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population.
- Is a snp
- In dbSNP
- SNPs on chromosome 17
- Has genotype
- Has population
- Uses omim
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- 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 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d