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: rs2000999
rs2000999
7 1.000 0.080 16 72074194 intron variant G/A snv 0.16 0.800 1.000 7 2010 2019
dbSNP: rs77303550
rs77303550
6 16 72045758 intron variant C/T snv 0.19 0.700 1.000 2 2018 2019
dbSNP: rs34042070
rs34042070
4 16 72067626 intron variant C/G snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs3794695
rs3794695
4 16 72063928 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs5471
rs5471
6 0.882 0.160 16 72054562 5 prime UTR variant A/C;G snv 7.9E-03 0.700 1.000 1 2018 2018