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: rs1169296
rs1169296
1 1.000 0.120 12 120990604 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs7310409
rs7310409
7 0.925 0.160 12 120987058 intron variant A/C;G;T snv 0.700 1.000 1 2015 2015