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: rs10405681
rs10405681
1 1.000 0.080 19 3634021 intron variant C/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs10419980
rs10419980
1 1.000 0.080 19 3685118 intron variant C/T snv 0.29 0.010 1.000 1 2018 2018
dbSNP: rs10432303
rs10432303
1 1.000 0.080 19 3656654 intron variant G/A snv 0.41 0.010 1.000 1 2018 2018
dbSNP: rs1476592
rs1476592
1 1.000 0.080 19 3679742 intron variant A/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs2074957
rs2074957
1 1.000 0.080 19 3653527 synonymous variant C/A;T snv 8.0E-06; 0.57 0.010 1.000 1 2018 2018
dbSNP: rs4432372
rs4432372
1 1.000 0.080 19 3698844 intron variant A/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs4807493
rs4807493
1 1.000 0.080 19 3631038 3 prime UTR variant A/G snv 0.84 0.010 1.000 1 2018 2018
dbSNP: rs8109485
rs8109485
1 1.000 0.080 19 3664096 intron variant A/G snv 0.21 0.010 1.000 1 2018 2018