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: rs10498676
rs10498676
3 0.925 0.040 6 11026766 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs12195587
rs12195587
1 6 10989709 synonymous variant G/A snv 0.12 0.11 0.700 1.000 1 2011 2011
dbSNP: rs1225737
rs1225737
1 6 10982419 3 prime UTR variant C/T snv 0.59 0.700 1.000 1 2011 2011
dbSNP: rs1321536
rs1321536
1 6 11018579 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1323739
rs1323739
1 6 11004328 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1570069
rs1570069
1 6 11017592 intron variant A/G snv 0.54 0.700 1.000 1 2011 2011
dbSNP: rs17675073
rs17675073
1 6 11008416 intron variant G/A snv 0.11 0.700 1.000 1 2011 2011
dbSNP: rs17764592
rs17764592
1 6 11002911 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2180725
rs2180725
1 6 11025187 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2236212
rs2236212
2 1.000 0.040 6 10994782 intron variant G/C snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs2281591
rs2281591
1 6 10990260 intron variant A/G snv 0.30 0.700 1.000 1 2011 2011
dbSNP: rs2295601
rs2295601
1 6 11005453 synonymous variant G/A snv 0.22 0.21 0.700 1.000 1 2011 2011
dbSNP: rs2295602
rs2295602
1 6 11005609 intron variant T/C snv 0.57 0.54 0.700 1.000 1 2011 2011
dbSNP: rs3734398
rs3734398
1 6 10982740 3 prime UTR variant T/C snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs3756963
rs3756963
4 0.882 0.200 6 11021921 intron variant T/C snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs3778166
rs3778166
1 6 11032931 intron variant G/A snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3798707
rs3798707
1 6 10991702 intron variant C/T snv 0.53 0.700 1.000 1 2011 2011
dbSNP: rs3798709
rs3798709
1 6 11001043 intron variant A/G snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3798710
rs3798710
1 6 11002550 intron variant G/C snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3798711
rs3798711
1 6 11002577 intron variant T/C snv 0.52 0.700 1.000 1 2011 2011
dbSNP: rs3798713
rs3798713
1 6 11008389 intron variant G/C snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs3798719
rs3798719
1 6 11036592 intron variant C/T snv 0.18 0.700 1.000 1 2011 2011
dbSNP: rs3798721
rs3798721
1 6 11039950 intron variant A/C snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs3798722
rs3798722
2 6 11040190 intron variant A/G snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs3798723
rs3798723
1 6 11041487 intron variant G/A snv 0.30 0.700 1.000 1 2011 2011