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: rs1033962
rs1033962
1 1.000 0.040 10 24927877 intron variant C/T snv 0.33 0.700 1.000 1 2015 2015
dbSNP: rs6482463
rs6482463
1 1.000 0.040 10 24924199 intron variant G/A snv 0.33 0.010 1.000 1 2015 2015