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: rs12908437
rs12908437
5 0.882 0.200 15 98744146 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs12911273
rs12911273
1 15 98752421 intron variant C/T snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs143193096
rs143193096
3 15 98916098 missense variant G/A;C snv 8.4E-05; 4.0E-06 0.700 1.000 1 2018 2018
dbSNP: rs4966024
rs4966024
3 0.925 0.120 15 98752341 intron variant G/A snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs59350108
rs59350108
1 15 98746378 intron variant G/C snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs6598541
rs6598541
3 0.925 0.120 15 98727906 intron variant A/G snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs6598542
rs6598542
3 0.925 0.120 15 98749827 intron variant G/A;T snv 0.700 1.000 1 2019 2019