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: rs1051730
rs1051730
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.700 1.000 4 2010 2012
dbSNP: rs667282
rs667282
13 0.790 0.120 15 78571130 intron variant T/C snv 0.28 0.700 1.000 4 2010 2012
dbSNP: rs11072766
rs11072766
2 15 78479204 intron variant C/G;T snv 0.700 1.000 3 2010 2010
dbSNP: rs11637630
rs11637630
6 0.882 0.080 15 78607377 intron variant G/A snv 0.71 0.700 1.000 3 2010 2010
dbSNP: rs12910984
rs12910984
8 0.827 0.080 15 78599285 intron variant G/A;C;T snv 0.700 1.000 3 2010 2010
dbSNP: rs12914385
rs12914385
18 0.790 0.160 15 78606381 intron variant C/A;T snv 0.800 1.000 3 2010 2017
dbSNP: rs16969968
rs16969968
37 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 0.700 1.000 3 2010 2012
dbSNP: rs200049096
rs200049096
1 15 78510715 intron variant -/T delins 1.4E-05 0.700 1.000 3 2010 2010
dbSNP: rs2036527
rs2036527
12 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 0.700 1.000 3 2010 2012
dbSNP: rs2036534
rs2036534
8 0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 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: rs2656069
rs2656069
5 0.882 0.080 15 78453365 intron variant C/G;T snv 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: rs3743078
rs3743078
7 0.807 0.160 15 78602417 intron variant C/A;G snv 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: rs6495308
rs6495308
8 0.851 0.160 15 78615314 intron variant T/C snv 0.29 0.700 1.000 3 2010 2010