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: rs4961
rs4961
27 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 0.100 0.842 38 1998 2020
dbSNP: rs4963
rs4963
6 0.827 0.120 4 2915035 missense variant C/G;T snv 0.20 0.18 0.020 1.000 2 2013 2016
dbSNP: rs1255327081
rs1255327081
1 4 2926062 missense variant A/G snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs16843452
rs16843452
1 4 2847441 intron variant C/T snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs372777117
rs372777117
1 4 2898494 missense variant A/G;T snv 4.0E-06; 1.2E-05 0.010 1.000 1 1998 1998