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: rs1011526
rs1011526
1 1.000 0.080 X 66196245 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs1091486
rs1091486
1 1.000 0.080 X 66219622 intron variant C/T snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs1264216
rs1264216
1 1.000 0.080 X 66215415 intron variant T/G snv 0.30 0.700 1.000 1 2012 2012
dbSNP: rs2206203
rs2206203
1 1.000 0.080 X 66195332 intron variant T/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs6624875
rs6624875
1 1.000 0.080 X 66188603 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs7054364
rs7054364
1 1.000 0.080 X 66172794 intron variant C/A snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs806607
rs806607
1 1.000 0.080 X 66207198 synonymous variant T/C snv 0.24 0.40 0.700 1.000 1 2012 2012
dbSNP: rs806608
rs806608
1 1.000 0.080 X 66208687 intron variant G/T snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs806610
rs806610
1 1.000 0.080 X 66213697 intron variant A/G snv 0.30 0.700 1.000 1 2012 2012