Disease: Congenital bilateral aplasia of vas deferens ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17107315
rs17107315
Entrez Id: 6690
Gene Symbol: SPINK1
SPINK1
CUI: C0403814
Disease:
Congenital bilateral aplasia of vas deferens 		0.010 GeneticVariation BEFREE Thus, common CFTR haplotypes modulate ICP and CBAVD susceptibility alone and in heterozygous CFTR and p.Asn34Ser mutation carriers. 21520337 2011