Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C0423112
Disease: Short palpebral fissure
Short palpebral fissure
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C3887499
Disease: Renal cyst
Renal cyst
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
CUI: C0281788
Disease: Biventricular hypertrophy
Biventricular hypertrophy
0.700 0
dbSNP: rs1213930919
rs1213930919
0.882 0.120 2 178577785 stop gained G/A snv
Morphological abnormality of the central nervous system
0.700 0