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: rs10947261
rs10947261
4 0.882 0.240 6 32405455 splice region variant G/T snv 0.11 0.700 1.000 1 2009 2009
dbSNP: rs1555115
rs1555115
1 1.000 0.080 6 32386743 intron variant C/G snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs17495612
rs17495612
1 1.000 0.080 6 32391654 non coding transcript exon variant T/C snv 0.16 0.700 1.000 1 2009 2009
dbSNP: rs2076530
rs2076530
17 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 0.700 1.000 1 2009 2009
dbSNP: rs2076533
rs2076533
3 0.882 0.200 6 32395750 intron variant C/T snv 0.40 0.700 1.000 1 2009 2009
dbSNP: rs3129900
rs3129900
3 0.882 0.200 6 32338202 intron variant G/T snv 0.83 0.700 1.000 1 2010 2010
dbSNP: rs3806156
rs3806156
5 0.827 0.280 6 32405921 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs4959093
rs4959093
4 0.882 0.200 6 32345320 intron variant T/C snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs539703
rs539703
4 0.882 0.200 6 32320685 intron variant A/C;T snv 0.700 1.000 1 2009 2009
dbSNP: rs544358
rs544358
2 0.925 0.120 6 32305381 intron variant G/C snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs574710
rs574710
4 0.882 0.200 6 32320413 intron variant T/C snv 0.34 0.700 1.000 1 2009 2009
dbSNP: rs6907322
rs6907322
2 1.000 0.080 6 32357168 intron variant G/A snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs910050
rs910050
2 0.925 0.120 6 32347877 intron variant G/C snv 0.42 0.700 1.000 1 2009 2009
dbSNP: rs926591
rs926591
4 0.882 0.200 6 32337913 intron variant C/A snv 0.33 0.700 1.000 1 2009 2009
dbSNP: rs9268302
rs9268302
2 1.000 0.080 6 32357040 intron variant C/T snv 0.29 0.700 1.000 1 2009 2009
dbSNP: rs9268402
rs9268402
5 0.827 0.200 6 32373576 intron variant G/A snv 0.45 0.700 1.000 1 2009 2009
dbSNP: rs9368716
rs9368716
4 0.882 0.200 6 32338313 intron variant G/A snv 0.39 0.700 1.000 1 2009 2009