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: rs150664883
rs150664883
2 18 37566243 intron variant C/A snv 5.7E-02 0.700 1.000 1 2015 2015
dbSNP: rs41475954
rs41475954
2 18 37505770 intron variant G/A snv 5.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs79828856
rs79828856
2 18 37456867 intron variant C/A snv 6.7E-02 0.700 1.000 1 2015 2015