Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs769022021
rs769022021
1 2 232850301 missense variant G/A snv 1.6E-05 4.2E-05 0.700 1.000 4 2008 2015
dbSNP: rs776898936
rs776898936
1 2 232791080 missense variant T/A snv 2.8E-05 1.4E-05 0.700 1.000 4 2008 2015
dbSNP: rs114013774
rs114013774
1 2 232847513 missense variant T/A;C snv 7.2E-05; 1.9E-04; 1.9E-05; 4.8E-06 3.1E-04 0.700 0
dbSNP: rs115735611
rs115735611
1 2 232791426 missense variant A/G snv 1.0E-04 7.7E-05 0.700 0
dbSNP: rs116074753
rs116074753
2 1.000 0.040 2 232794835 missense variant A/C;G snv 3.9E-04; 8.0E-06 0.700 0
dbSNP: rs1171688751
rs1171688751
2 1.000 0.040 2 232756289 missense variant A/G snv 4.3E-06 2.1E-05 0.700 0
dbSNP: rs118203903
rs118203903
2 1.000 0.040 2 232809731 missense variant C/G snv 0.700 0
dbSNP: rs118203904
rs118203904
2 1.000 0.040 2 232790817 missense variant A/G snv 2.3E-04 6.3E-05 0.700 0
dbSNP: rs1384919564
rs1384919564
1 2 232794882 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs141225775
rs141225775
1 2 232790803 missense variant C/G;T snv 1.2E-05; 1.6E-04 0.700 0
dbSNP: rs148277228
rs148277228
1 2 232791124 missense variant T/A snv 5.5E-04 4.5E-04 0.700 0
dbSNP: rs72554080
rs72554080
3 0.925 0.040 2 232747740 missense variant A/G snv 2.6E-04 3.2E-04 0.700 0
dbSNP: rs748538823
rs748538823
1 2 232819834 missense variant C/G;T snv 4.1E-06; 5.3E-05 0.700 0