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: rs11072766
rs11072766
2 15 78479204 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs200049096
rs200049096
1 15 78510715 intron variant -/T delins 1.4E-05 0.700 1.000 3 2010 2010
dbSNP: rs2568483
rs2568483
2 15 78460001 intron variant G/A;T snv 0.700 1.000 3 2010 2010
dbSNP: rs2568488
rs2568488
2 15 78444251 intron variant T/A snv 0.78 0.700 1.000 3 2010 2010
dbSNP: rs2656071
rs2656071
2 15 78453001 intron variant T/A snv 0.79 0.700 1.000 3 2010 2010
dbSNP: rs2656073
rs2656073
2 15 78449934 intron variant T/A;G snv 0.700 1.000 3 2010 2010
dbSNP: rs2869032
rs2869032
2 15 78422219 regulatory region variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs2869045
rs2869045
3 15 78426557 regulatory region variant T/C snv 0.78 0.700 1.000 3 2010 2010
dbSNP: rs2938674
rs2938674
2 15 78465571 intron variant C/A snv 0.23 0.700 1.000 3 2010 2010
dbSNP: rs3813570
rs3813570
2 15 78540490 5 prime UTR variant T/C snv 0.27 0.700 1.000 3 2010 2010
dbSNP: rs4461039
rs4461039
2 15 78525105 intron variant A/T snv 0.27 0.700 1.000 3 2010 2010
dbSNP: rs4887069
rs4887069
2 15 78616728 intron variant A/G snv 0.30 0.700 1.000 3 2010 2010
dbSNP: rs5019044
rs5019044
2 15 78503940 upstream gene variant T/A snv 0.21 0.700 1.000 3 2010 2010
dbSNP: rs637137
rs637137
3 15 78581634 intron variant T/A snv 0.29 0.700 1.000 3 2010 2010
dbSNP: rs7163730
rs7163730
3 15 78522339 intron variant A/G snv 0.25 0.700 1.000 3 2010 2010
dbSNP: rs7164594
rs7164594
2 15 78510715 intron variant C/T snv 0.32 0.700 1.000 3 2010 2010
dbSNP: rs9788682
rs9788682
2 15 78510244 intron variant G/A;T snv 0.700 1.000 3 2010 2010
dbSNP: rs1021071
rs1021071
3 15 78675837 intron variant G/C snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11072774
rs11072774
1 15 78660355 intron variant C/T snv 0.20 0.700 1.000 2 2010 2010
dbSNP: rs11072785
rs11072785
3 15 78675887 intron variant C/T snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11072787
rs11072787
1 15 78680635 intron variant T/C snv 0.34 0.700 1.000 2 2010 2010
dbSNP: rs11072791
rs11072791
3 15 78704734 intron variant C/A snv 0.29 0.700 1.000 2 2010 2010
dbSNP: rs11629637
rs11629637
3 15 78726682 intron variant C/T snv 0.31 0.700 1.000 2 2010 2010
dbSNP: rs11634351
rs11634351
3 15 78652376 intron variant G/A snv 0.28 0.700 1.000 2 2010 2010
dbSNP: rs11636605
rs11636605
1 15 78636536 intron variant A/G snv 0.63 0.700 1.000 2 2010 2010