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: rs2281808
rs2281808
4 0.925 0.160 20 1629905 intron variant T/A;C snv 0.820 1.000 3 2009 2019
dbSNP: rs6043409
rs6043409
2 1.000 0.120 20 1635560 missense variant A/G snv 0.73 0.72 0.700 1.000 1 2015 2015