Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9284390
rs9284390
ROCK1P1 ; MIR8078
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		0.010 GeneticVariation BEFREE We linked this form of ED to human chromosome 18p11.32-p11.31 flanked by the SNPs rs9284390 (0.113Mb) and rs4797100 (3.14 Mb). 26115030

2015