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: rs1432033565
rs1432033565
1 1.000 0.040 22 20242258 missense variant C/G;T snv 4.7E-06; 4.7E-06 0.710 1.000 1 2017 2017
dbSNP: rs74315508
rs74315508
2 1.000 0.040 22 20242778 missense variant G/A;C snv 3.5E-04; 8.1E-06 0.700 1.000 3 2004 2017
dbSNP: rs74315509
rs74315509
2 1.000 0.040 22 20242546 missense variant C/T snv 2.4E-05 7.0E-05 0.700 1.000 3 2004 2017
dbSNP: rs754793885
rs754793885
1 1.000 0.040 22 20242454 missense variant G/A;T snv 1.6E-05; 1.2E-05 0.700 1.000 3 2004 2017
dbSNP: rs200119628
rs200119628
1 1.000 0.040 22 20241938 missense variant G/A snv 3.0E-04 2.4E-04 0.700 0
dbSNP: rs748655075
rs748655075
1 1.000 0.040 22 20242004 missense variant G/A snv 4.5E-05 2.8E-05 0.700 0
dbSNP: rs779384862
rs779384862
1 1.000 0.040 22 20242003 missense variant C/G;T snv 7.8E-05 0.700 0