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: rs1345203
rs1345203
2 2 111496274 intron variant T/C;G snv 0.700 1.000 2 2019 2019
dbSNP: rs59043281
rs59043281
1 2 111503453 intron variant G/A snv 0.22 0.700 1.000 1 2019 2019