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: rs3129900
rs3129900
3 0.882 0.200 6 32338202 intron variant G/T snv 0.83 0.700 1.000 1 2010 2010
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