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: rs2526376
rs2526376
1 17 58349781 intron variant A/C snv 0.58 0.700 1.000 2 2018 2018
dbSNP: rs757485
rs757485
1 17 58347349 intron variant T/C snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs8070135
rs8070135
1 17 58381702 intron variant G/A snv 0.30 0.700 1.000 1 2018 2018