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: rs16982520
rs16982520
4 1.000 0.040 20 59183665 intron variant A/G snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs6015450
rs6015450
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs6026740
rs6026740
3 20 59165293 intron variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs79263055
rs79263055
2 20 59175423 intron variant T/A;C snv 0.700 1.000 1 2018 2018