Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs760330563
rs760330563
DCTN6
CUI: C0001206
Disease: Acromegaly
Acromegaly 		0.010 GeneticVariation BEFREE The I119T substitution occurred in a female patient with acromegaly. p27(I119T) shows an abnormal migration pattern by SDS-PAGE. 22291433

2012