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: rs115179432
rs115179432
2 2 33123612 intron variant A/G snv 5.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs116713089
rs116713089
1 2 33134498 5 prime UTR variant G/A snv 5.4E-02 4.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs34447926
rs34447926
1 2 33363802 intron variant A/C snv 0.34 0.700 1.000 1 2018 2018