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: rs6664388
rs6664388
1 1 15581747 intron variant C/T snv 0.30 0.700 1.000 2 2019 2019
dbSNP: rs10159261
rs10159261
1 1 15586492 non coding transcript exon variant G/T snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs12124078
rs12124078
3 1 15543404 intron variant A/G snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs45619934
rs45619934
1 1 15585452 intron variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6667182
rs6667182
1 1 15588050 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7546668
rs7546668
2 1 15528628 intron variant G/A;C snv 0.31 0.700 1.000 1 2017 2017