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: rs1152578
rs1152578
1 1.000 0.040 14 64230319 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs915057
rs915057
1 1.000 0.040 14 64219489 intron variant A/G;T snv 0.700 1.000 1 2018 2018