Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs281875329
rs281875329
ACTG1 ; FSCN2
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs765574676
rs765574676
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs377650415
rs377650415
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1561843914
rs1561843914
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1561805689
rs1561805689
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561790371
rs1561790371
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1561543496
rs1561543496
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1561441451
rs1561441451
ADGRV1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs777476179
rs777476179
ALMS1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519338
rs1057519338
AMMECR1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs765498367
rs765498367
AMMECR1 ; LOC105373312
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1565331646
rs1565331646
ANAPC15 ; LRTOMT
CUI: C1384666
Disease: hearing impairment
hearing impairment 		AGCTC 0.700 GeneticVariation CLINVAR

dbSNP: rs886039902
rs886039902
ANKRD11
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs878855327
rs878855327
ANKRD11
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs387907141
rs387907141
ARID1B
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs373145711
rs373145711
ASXL1
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs121908354
rs121908354
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.710 CausalMutation CLINVAR

dbSNP: rs758382198
rs758382198
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs756147087
rs756147087
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1564791773
rs1564791773
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1554877797
rs1554877797
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1554874900
rs1554874900
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1554874879
rs1554874879
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1554871816
rs1554871816
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		C 0.700 CausalMutation CLINVAR

dbSNP: rs1390562340
rs1390562340
CDH23
CUI: C1384666
Disease: hearing impairment
hearing impairment 		G 0.700 CausalMutation CLINVAR