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: rs2300747
rs2300747
1 0.882 0.200 1 116561593 intron variant A/G snv 0.19 0.820 1.000 3 2009 2018
dbSNP: rs1335532
rs1335532
1 1.000 0.080 1 116558335 intron variant A/G snv 0.28 0.810 1.000 4 2009 2018