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 0.800 1.000 10 2009 2019
dbSNP: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.800 1.000 7 2012 2019
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 6 2009 2019
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 5 2008 2019
dbSNP: rs261334
rs261334
5 15 58434545 intron variant G/C snv 0.73 0.800 1.000 5 2010 2019
dbSNP: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 5 2008 2019
dbSNP: rs8034802
rs8034802
5 15 58432593 intron variant T/A snv 0.33 0.800 1.000 4 2011 2019
dbSNP: rs1077835
rs1077835
5 15 58431227 intron variant A/G snv 0.34 0.800 1.000 3 2013 2019
dbSNP: rs16940212
rs16940212
4 1.000 0.040 15 58401821 intron variant G/A;T snv 0.800 1.000 3 2011 2019
dbSNP: rs261332
rs261332
20 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.800 1.000 3 2012 2018
dbSNP: rs261342
rs261342
5 15 58438954 intron variant G/A;C;T snv 0.800 1.000 3 2012 2019
dbSNP: rs261336
rs261336
5 15 58450219 intron variant G/A snv 0.81 0.800 1.000 2 2012 2018
dbSNP: rs588136
rs588136
5 15 58438299 intron variant C/G;T snv 0.800 1.000 2 2012 2013
dbSNP: rs1077834
rs1077834
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 5 2010 2019
dbSNP: rs261291
rs261291
5 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 5 2015 2019
dbSNP: rs13329672
rs13329672
4 15 58407738 intron variant C/T snv 0.31 0.700 1.000 3 2018 2019
dbSNP: rs1601935
rs1601935
4 15 58379566 intron variant G/T snv 0.60 0.700 1.000 2 2018 2019
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: rs118146059
rs118146059
1 15 58252574 intron variant T/C snv 1.7E-03 0.700 1.000 1 2018 2018
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: rs12148399
rs12148399
2 15 58289171 intron variant T/A snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12148780
rs12148780
2 1.000 0.080 15 58289090 intron variant A/G snv 0.14 0.700 1.000 1 2019 2019