BIVM-ERCC5, BIVM-ERCC5 readthrough, 100533467

N. diseases: 15; N. variants: 38
Disease: Dysarthria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518813
rs1057518813
Entrez Id: 2073;100533467
Gene Symbol: ERCC5;BIVM-ERCC5
ERCC5;BIVM-ERCC5
CUI: C0013362
Disease:
Dysarthria 		A 0.700 GeneticVariation CLINVAR