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: rs10911251
rs10911251
9 0.790 0.080 1 183112059 intron variant A/C snv 0.37 0.700 1.000 2 2013 2019
dbSNP: rs4546885
rs4546885
9 0.790 0.080 1 183056420 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6678517
rs6678517
10 0.776 0.080 1 183033504 intron variant A/G;T snv 0.700 1.000 1 2019 2019