Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060499590
rs1060499590
SMPX
T 0.700 GeneticVariation CLINVAR Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment. 21549342

2011
dbSNP: rs1060499590
rs1060499590
SMPX
T 0.700 GeneticVariation CLINVAR Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. 21549336

2011
dbSNP: rs387906706
rs387906706
SMPX
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906707
rs387906707
SMPX
A 0.700 CausalMutation CLINVAR

dbSNP: rs387906708
rs387906708
SMPX
A 0.700 CausalMutation CLINVAR

dbSNP: rs398122848
rs398122848
SMPX
T 0.700 CausalMutation CLINVAR

dbSNP: rs398122930
rs398122930
SMPX
T 0.700 CausalMutation CLINVAR