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: rs10411210
rs10411210
13 0.742 0.160 19 33041394 intron variant C/T snv 0.22 0.700 1.000 3 2008 2019
dbSNP: rs13343954
rs13343954
9 0.790 0.080 19 33036982 intron variant T/C snv 0.18 0.700 1.000 1 2014 2014
dbSNP: rs28840750
rs28840750
10 0.776 0.080 19 33029021 intron variant T/G snv 7.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs73039434
rs73039434
9 0.790 0.080 19 33034013 intron variant T/G snv 0.13 0.700 1.000 1 2019 2019