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: rs1004870
rs1004870
1 1 41905116 intron variant C/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs2147904
rs2147904
2 1 41905743 intron variant T/C snv 0.50 0.700 1.000 1 2016 2016