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: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.700 1.000 6 2009 2013
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.700 1.000 3 2009 2012
dbSNP: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.700 1.000 3 2012 2012
dbSNP: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.700 1.000 3 2008 2012
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.700 1.000 2 2008 2012
dbSNP: rs8034802
rs8034802
5 15 58432593 intron variant T/A snv 0.33 0.700 1.000 2 2012 2012
dbSNP: rs1077835
rs1077835
5 15 58431227 intron variant A/G snv 0.34 0.700 1.000 1 2013 2013
dbSNP: rs11632618
rs11632618
3 15 58432507 intron variant G/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs11635491
rs11635491
4 15 58427542 intron variant G/A snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs11855284
rs11855284
3 15 58396988 intron variant T/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs11856159
rs11856159
4 15 58406811 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11858164
rs11858164
3 15 58450532 intron variant T/G snv 0.39 0.700 1.000 1 2008 2008
dbSNP: rs16940212
rs16940212
4 1.000 0.040 15 58401821 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs17190517
rs17190517
3 15 58436945 intron variant C/T snv 0.37 0.33 0.700 1.000 1 2012 2012
dbSNP: rs17269264
rs17269264
3 15 58446561 intron variant G/A snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs17269271
rs17269271
3 15 58447562 intron variant G/C snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs261332
rs261332
20 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs261334
rs261334
5 15 58434545 intron variant G/C snv 0.73 0.700 1.000 1 2010 2010
dbSNP: rs261336
rs261336
5 15 58450219 intron variant G/A snv 0.81 0.700 1.000 1 2012 2012
dbSNP: rs261338
rs261338
5 15 58442806 intron variant A/G snv 0.83 0.700 1.000 1 2012 2012
dbSNP: rs261341
rs261341
4 15 58439368 intron variant A/G snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs261342
rs261342
5 15 58438954 intron variant G/A;C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs415799
rs415799
4 15 58398555 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs473224
rs473224
5 15 58445142 intron variant T/A;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4774297
rs4774297
3 15 58428232 intron variant C/A snv 0.43 0.700 1.000 1 2012 2012