Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C4021765
Disease: Morphological abnormality of the central nervous system
Morphological abnormality of the central nervous system 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C3887499
Disease: Renal cyst
Renal cyst 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C0281788
Disease: Biventricular hypertrophy
Biventricular hypertrophy 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1213930919
rs1213930919
TTN ; TTN-AS1
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis 		A 0.700 GeneticVariation CLINVAR