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: rs5029937
rs5029937
4 0.882 0.160 6 137874014 intron variant G/T snv 0.13 0.740 1.000 1 2009 2017
dbSNP: rs5029924
rs5029924
2 0.851 0.200 6 137866361 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs5029949
rs5029949
2 0.925 0.120 6 137876369 intron variant A/G snv 8.1E-02 0.700 1.000 1 2012 2012