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: rs1354115
rs1354115
1 1.000 0.040 9 2983774 intron variant C/A;T snv 0.700 1.000 2 2018 2019
dbSNP: rs7044150
rs7044150
1 1.000 0.040 9 2982931 intron variant T/A;C;G snv 0.700 1.000 1 2016 2016