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: rs1014242
rs1014242
1 7 32232693 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs10226228
rs10226228
1 7 32276001 intron variant A/G snv 0.38 0.700 1.000 1 2010 2010
dbSNP: rs10236197
rs10236197
2 7 32252149 intron variant T/C snv 0.41 0.700 1.000 1 2010 2010
dbSNP: rs10259431
rs10259431
1 7 32241785 intron variant C/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs10264177
rs10264177
1 7 32331250 intron variant A/G snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs10951331
rs10951331
1 7 32314762 intron variant A/G snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs12531858
rs12531858
1 7 32300487 intron variant C/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs12540232
rs12540232
1 7 32283349 intron variant T/C snv 0.40 0.700 1.000 1 2010 2010
dbSNP: rs1450869
rs1450869
1 7 32272060 intron variant G/T snv 0.57 0.700 1.000 1 2010 2010
dbSNP: rs1450870
rs1450870
1 7 32272114 intron variant T/A;C;G snv 0.50 0.700 1.000 1 2010 2010
dbSNP: rs1476765
rs1476765
1 7 32280846 intron variant G/T snv 0.56 0.700 1.000 1 2010 2010
dbSNP: rs215596
rs215596
1 7 32286761 intron variant A/G snv 0.50 0.700 1.000 1 2010 2010
dbSNP: rs215599
rs215599
1 7 32290517 intron variant C/T snv 0.50 0.700 1.000 1 2010 2010
dbSNP: rs215600
rs215600
2 7 32294030 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs215601
rs215601
1 7 32294309 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs215605
rs215605
2 1.000 0.040 7 32297353 intron variant G/T snv 0.54 0.700 1.000 1 2010 2010
dbSNP: rs215607
rs215607
2 7 32298725 missense variant G/A snv 0.79 0.77 0.700 1.000 1 2010 2010
dbSNP: rs215610
rs215610
1 7 32299982 intron variant G/A snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs215614
rs215614
3 7 32307723 intron variant G/A snv 0.62 0.700 1.000 1 2010 2010
dbSNP: rs215622
rs215622
1 7 32318047 intron variant C/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs215625
rs215625
1 7 32318701 intron variant G/A snv 0.58 0.700 1.000 1 2010 2010
dbSNP: rs215629
rs215629
1 7 32320852 intron variant G/C;T snv 0.700 1.000 1 2010 2010
dbSNP: rs215632
rs215632
1 7 32328912 intron variant A/G snv 0.53 0.700 1.000 1 2010 2010
dbSNP: rs215634
rs215634
2 7 32329536 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs215635
rs215635
1 7 32330608 intron variant C/T snv 0.53 0.700 1.000 1 2010 2010