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: rs261342
rs261342
5 15 58438954 intron variant G/A;C;T snv 0.800 1.000 3 2012 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 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: rs473224
rs473224
5 15 58445142 intron variant T/A;G snv 0.700 1.000 2 2009 2012
dbSNP: rs10518982
rs10518982
3 15 58507555 intron variant A/G snv 2.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10518983
rs10518983
1 15 58520578 intron variant C/T snv 5.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs12324244
rs12324244
1 15 58520749 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs16940391
rs16940391
3 15 58507449 intron variant C/A;G snv 0.700 1.000 1 2012 2012
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: rs485538
rs485538
5 15 58448978 intron variant C/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs485671
rs485671
5 15 58448935 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs8033940
rs8033940
5 15 58432643 intron variant G/A snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs8034802
rs8034802
5 15 58432593 intron variant T/A snv 0.33 0.700 1.000 1 2012 2012