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: rs1007738
rs1007738
1 11 46827809 intron variant G/A snv 0.64 0.800 1.000 1 2009 2009
dbSNP: rs10838622
rs10838622
1 11 46834985 intron variant T/C snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs61884327
rs61884327
1 11 46745340 intron variant T/C snv 8.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs61884328
rs61884328
1 11 46761885 intron variant T/C snv 8.4E-02 0.700 1.000 1 2018 2018