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: rs2911463
rs2911463
1 1.000 0.040 16 88769137 intron variant G/A;C snv 0.700 1.000 2 2018 2019
dbSNP: rs8053350
rs8053350
1 1.000 0.040 16 88727995 intron variant G/A;C snv 0.700 1.000 1 2018 2018