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: rs9405157
rs9405157
1 6 1988690 intron variant T/C snv 0.24 0.700 1.000 2 2018 2018
dbSNP: rs3778523
rs3778523
1 6 1777530 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs6914086
rs6914086
1 6 2095801 intron variant T/C snv 0.58 0.700 1.000 1 2018 2018
dbSNP: rs722585
rs722585
2 6 1775629 intron variant G/A snv 0.25 0.700 1.000 1 2018 2018
dbSNP: rs9378319
rs9378319
1 6 2053443 intron variant T/C snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs9378671
rs9378671
1 6 2040937 intron variant T/C snv 0.21 0.700 1.000 1 2018 2018