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: rs12901499
rs12901499
3 0.882 0.040 15 67078107 intron variant G/A snv 0.45 0.040 1.000 4 2018 2018
dbSNP: rs12102171
rs12102171
1 1.000 0.040 15 67132695 intron variant C/T snv 0.22 0.010 1.000 1 2015 2015
dbSNP: rs12595334
rs12595334
1 1.000 0.040 15 67192818 3 prime UTR variant C/T snv 0.19 0.010 1.000 1 2014 2014
dbSNP: rs12901071
rs12901071
3 0.882 0.160 15 67078051 intron variant A/G snv 0.25 0.010 1.000 1 2017 2017
dbSNP: rs2289263
rs2289263
3 0.925 0.120 15 67146869 intron variant T/G snv 0.43 0.010 1.000 1 2015 2015
dbSNP: rs3743342
rs3743342
1 1.000 0.040 15 67193329 3 prime UTR variant C/T snv 0.20 0.010 1.000 1 2014 2014
dbSNP: rs6494629
rs6494629
2 0.925 0.120 15 67081773 intron variant C/T snv 0.52 0.010 1.000 1 2015 2015
dbSNP: rs8031440
rs8031440
1 1.000 0.040 15 67191641 3 prime UTR variant G/A snv 0.19 0.010 1.000 1 2014 2014