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: rs10189857
rs10189857
6 1.000 0.080 2 60486100 intron variant A/G snv 0.42 0.700 1.000 2 2018 2019
dbSNP: rs13019832
rs13019832
3 2 60483436 intron variant G/A snv 0.39 0.700 1.000 2 2018 2019
dbSNP: rs7599488
rs7599488
4 0.925 0.120 2 60491212 intron variant C/T snv 0.42 0.700 1.000 2 2018 2019
dbSNP: rs7565301
rs7565301
3 1.000 0.080 2 60496131 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs7581162
rs7581162
3 2 60477349 intron variant T/A snv 0.49 0.700 1.000 1 2017 2017