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: rs10840138
rs10840138
2 11 1980665 intron variant T/C snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs12575654
rs12575654
2 11 1989738 intron variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs217719
rs217719
3 11 1973993 intron variant G/A snv 0.27 0.700 1.000 1 2018 2018