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: rs9308315
rs9308315
1 12 102410115 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs972936
rs972936
12 0.807 0.200 12 102431143 intron variant T/C snv 0.70 0.700 1.000 1 2019 2019