Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1784594
rs1784594
PRKN
0.010 GeneticVariation BEFREE In female cases, the T allele frequency of rs1784594 was significantly lower in DNS patients compared to female controls (OR = 1.48, 95%CI: 1.01 - 2.17). 24063657

2013
dbSNP: rs34886500
rs34886500
CDKN2A
0.010 GeneticVariation BEFREE In one family where the proband had a P48L mutation in CDKN2A exon 1, the DNS phenotype was studied in detail. 10338331

1999
dbSNP: rs768477694
rs768477694
CDK4
0.010 GeneticVariation BEFREE In one family where the proband had a P48L mutation in CDKN2A exon 1, the DNS phenotype was studied in detail. 10338331

1999