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: rs1131690775
rs1131690775
1 1.000 0.040 4 169590736 missense variant A/C snv 0.700 1.000 1 2017 2017
dbSNP: rs200161705
rs200161705
5 0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs34324114
rs34324114
1 1.000 0.040 4 169477323 missense variant A/C snv 4.6E-03 4.1E-03 0.700 1.000 1 2017 2017
dbSNP: rs377607698
rs377607698
1 1.000 0.040 4 169424635 missense variant G/A;C snv 2.4E-05; 4.0E-06 0.700 1.000 1 2017 2017
dbSNP: rs772747361
rs772747361
1 1.000 0.040 4 169585461 missense variant C/A;T snv 2.0E-05 0.700 1.000 1 2017 2017
dbSNP: rs776098853
rs776098853
1 1.000 0.040 4 169508292 missense variant A/T snv 1.0E-04 6.3E-05 0.700 1.000 1 2017 2017