rs1172682117, ERG

N. diseases: 1
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Pain
CUI: C0030193
Disease: Pain
0.010 GeneticVariation BEFREE A heterozygous single base-pain substitution in exon 5 (408C --> A) was detected in all affected patients. 15823919 2005