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: rs4333130
rs4333130
1 1.000 0.040 4 80028675 intron variant C/G;T snv 0.820 1.000 3 2010 2016
dbSNP: rs4389526
rs4389526
1 1.000 0.040 4 80025321 intron variant T/A snv 0.59 0.810 1.000 2 2011 2018
dbSNP: rs11098964
rs11098964
5 0.827 0.120 4 79966815 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs6534639
rs6534639
2 0.925 0.080 4 79900765 downstream gene variant C/A snv 0.49 0.020 0.500 2 2016 2018
dbSNP: rs12504282
rs12504282
2 1.000 0.040 4 80005847 intron variant C/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs4690127
rs4690127
1 1.000 0.040 4 79929167 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs6823031
rs6823031
1 1.000 0.040 4 79935302 intron variant C/T snv 0.010 1.000 1 2016 2016