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: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 6 2012 2019
dbSNP: rs1532085
rs1532085
13 0.882 0.080 15 58391167 intron variant A/G;T snv 0.800 1.000 4 2010 2019
dbSNP: rs261342
rs261342
5 15 58438954 intron variant G/A;C;T snv 0.800 1.000 3 2012 2019
dbSNP: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 3 2008 2018
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 2 2009 2018
dbSNP: rs261332
rs261332
20 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.800 1.000 2 2012 2016
dbSNP: rs588136
rs588136
5 15 58438299 intron variant C/G;T snv 0.800 1.000 2 2012 2017
dbSNP: rs1077835
rs1077835
5 15 58431227 intron variant A/G snv 0.34 0.700 1.000 5 2015 2019
dbSNP: rs1077834
rs1077834
5 15 58431280 intron variant T/C snv 0.34 0.700 1.000 2 2018 2019
dbSNP: rs261291
rs261291
5 1.000 0.080 15 58387979 intron variant T/A;C snv 0.700 1.000 2 2018 2018
dbSNP: rs473224
rs473224
5 15 58445142 intron variant T/A;G snv 0.700 1.000 2 2009 2012
dbSNP: rs7350789
rs7350789
4 15 58387469 intron variant G/A snv 0.35 0.700 1.000 2 2018 2019
dbSNP: rs11856159
rs11856159
4 15 58406811 intron variant C/A;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs13329672
rs13329672
4 15 58407738 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1601935
rs1601935
4 15 58379566 intron variant G/T snv 0.60 0.700 1.000 1 2018 2018
dbSNP: rs166358
rs166358
2 15 58388606 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2043082
rs2043082
5 15 58382109 intron variant G/A snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs2043085
rs2043085
9 0.827 0.080 15 58388755 intron variant T/C snv 0.54 0.700 1.000 1 2009 2009
dbSNP: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 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 2018 2018
dbSNP: rs261336
rs261336
5 15 58450219 intron variant G/A snv 0.81 0.700 1.000 1 2009 2009
dbSNP: rs261338
rs261338
5 15 58442806 intron variant A/G snv 0.83 0.700 1.000 1 2012 2012
dbSNP: rs397923
rs397923
2 15 58399919 intron variant A/T snv 0.60 0.700 1.000 1 2009 2009
dbSNP: rs415799
rs415799
4 15 58398555 intron variant G/A snv 0.38 0.700 1.000 1 2009 2009
dbSNP: rs485538
rs485538
5 15 58448978 intron variant C/G;T snv 0.700 1.000 1 2012 2012