BLMH, bleomycin hydrolase, 642

N. diseases: 22; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16965645
rs16965645
Entrez Id: 642
Gene Symbol: BLMH
BLMH
CUI: C0027404
Disease:
Narcolepsy 		0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
dbSNP: rs1050565
rs1050565
Entrez Id: 642
Gene Symbol: BLMH
BLMH
CUI: C0030193
Disease:
Pain 		0.010 GeneticVariation BEFREE The <i>BLMH</i> rs1050565 G/G genotype was found to be associated with pain, and the <i>GSTP1</i> G/G genotype was linked infection (<i>p</i> < 0.05). 30914949 2019
dbSNP: rs1050565
rs1050565
Entrez Id: 642
Gene Symbol: BLMH
BLMH
CUI: C0002395
Disease:
Alzheimer's Disease 		0.010 GeneticVariation BEFREE Meta-analyses on AD association with BACE1 exon 5, BACE1 intron 5, FE65 intron 13, CYP46 intron 2, alpha(1)-antichymotrypsine Ala17Thr, bleomycin hydrolase I443V, lectin-like oxidized low-density lipoprotein receptor (OLR1) 3'-UTR (+1071) and (+1073), and very-low-density lipoprotein receptor (VLDLR) 5'-UTR (CGG-repeat) polymorphisms. 17854420 2008