rs11615866
This is a intergenic variant variant in the LOC105369617 gene.
▶Research that mentions this SNP (1)
▶A genome‐wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic painAssociationN=3,063Meng W. et al.(2015)· European Journal of Pain
A genome‐wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain
AssociationN=3,063Meng W. et al.(2015)· European Journal of Pain
Genome-wide association study of 572 diabetic neuropathic pain cases and 2491 controls identified a cluster near GFRA2 on chromosome 8p21.3 with the strongest association at rs17428041 (p=1.77×10⁻⁷, OR=0.67). The C allele was protective against neuropathic pain. Estimated narrow-sense heritability was 11.00%, suggesting neuropathic pain is a modestly heritable trait.
Traits studied:Diabetic neuropathic painPeripheral neuropathy
This variant is in our database but has no known associations or PRS memberships yet.
Gene information from NCBI Gene. Variant classifications from ClinVar.
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