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: rs6511720
rs6511720
7 0.790 0.120 19 11091630 intron variant G/T snv 0.12 0.710 1.000 2 2013 2018
dbSNP: rs2738447
rs2738447
1 1.000 0.040 19 11116804 intron variant A/C snv 0.65 0.700 1.000 1 2018 2018