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: rs3757173
rs3757173
1 1.000 0.080 6 137869017 intron variant A/G snv 0.20 0.720 1.000 3 2012 2016
dbSNP: rs5029924
rs5029924
4 0.851 0.200 6 137866361 intron variant C/T snv 0.13 0.700 1.000 1 2017 2017