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: rs6443750
rs6443750
1 3 181611894 intron variant T/C snv 0.87 0.700 1.000 2 2019 2019
dbSNP: rs1805207
rs1805207
1 3 181057346 intron variant C/T snv 0.74 0.700 1.000 1 2019 2019