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: rs6015450
rs6015450
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs459588
rs459588
2 20 59139712 intron variant A/C snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs6026740
rs6026740
3 20 59165293 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs6026748
rs6026748
3 20 59170760 intron variant G/A snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs73306888
rs73306888
2 20 59173534 intron variant G/A snv 0.14 0.700 1.000 1 2018 2018