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: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C1845019
Disease: Left ventricular septal hypertrophy
Left ventricular septal hypertrophy
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C4021810
Disease: Abnormal location of ears
Abnormal location of ears
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C1848395
Disease: Large for gestational age
Large for gestational age
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C1854469
Disease: Noonan Syndrome 2
Noonan Syndrome 2
0.700 1.000 1 2018 2018
dbSNP: rs1034395178
rs1034395178
0.716 0.480 22 20996071 stop gained C/A;T snv 4.0E-06; 8.0E-06
CUI: C1861324
Disease: Short philtrum
Short philtrum
0.700 1.000 1 2018 2018