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: 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 2 2012 2018
dbSNP: rs588136
rs588136
5 15 58438299 intron variant C/G;T snv 0.700 1.000 2 2012 2013
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 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: rs473224
rs473224
5 15 58445142 intron variant T/A;G snv 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: rs572410
rs572410
4 15 58449185 intron variant C/G;T snv 0.700 1.000 1 2012 2012