Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs201621853
rs201621853
Entrez Id: 3489
Gene Symbol: IGFBP6
IGFBP6
CUI: C1611743
Disease:
Familial (FPAH) 		0.010 GeneticVariation BEFREE The c.T430C (p.S144P) variant of IGFBP6 was identified as the likely causal variant associated with increased risk of familial disc degeneration in the studied pedigree. 28829625 2017
dbSNP: rs201621853
rs201621853
Entrez Id: 3489
Gene Symbol: IGFBP6
IGFBP6
CUI: C0158266
Disease:
Intervertebral Disc Degeneration 		0.010 GeneticVariation BEFREE The c.T430C (p.S144P) variant of IGFBP6 was identified as the likely causal variant associated with increased risk of familial disc degeneration in the studied pedigree. 28829625 2017