Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs76992529
rs76992529
TTR
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.780 CausalMutation CLINVAR

dbSNP: rs902082118
rs902082118
CSRP3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039136
rs886039136
GLA ; RPL36A-HNRNPH2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs876657670
rs876657670
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs869320740
rs869320740
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		G 0.700 CausalMutation CLINVAR

dbSNP: rs869312054
rs869312054
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs869025496
rs869025496
PKP2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs794729354
rs794729354
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 CausalMutation CLINVAR

dbSNP: rs794728826
rs794728826
RYR2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs778127887
rs778127887
TMEM43
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs774316050
rs774316050
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		C 0.700 CausalMutation CLINVAR

dbSNP: rs769665204
rs769665204
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs766265889
rs766265889
TTN ; TTN-AS1
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs751392310
rs751392310
MYL2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs730881119
rs730881119
TNNT2
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		TG 0.700 CausalMutation CLINVAR

dbSNP: rs730881069
rs730881069
TNNI3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880903
rs730880903
MYH7
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs730880895
rs730880895
MYH7
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs730880719
rs730880719
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		T 0.700 CausalMutation CLINVAR

dbSNP: rs730880718
rs730880718
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		C 0.700 CausalMutation CLINVAR

dbSNP: rs730880717
rs730880717
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		C 0.700 CausalMutation CLINVAR

dbSNP: rs730880715
rs730880715
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		C 0.700 CausalMutation CLINVAR

dbSNP: rs730880714
rs730880714
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		G 0.700 CausalMutation CLINVAR

dbSNP: rs730880689
rs730880689
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		TCATGGTCAGCCAGTTC 0.700 CausalMutation CLINVAR

dbSNP: rs730880675
rs730880675
MYBPC3
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		G 0.700 CausalMutation CLINVAR