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: rs59791349
rs59791349
1 20 46975185 intron variant C/T snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs6063050
rs6063050
2 20 46975601 intron variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs6066141
rs6066141
1 20 46968907 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018