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: rs4140993
rs4140993
1 12 1780116 intron variant T/G snv 5.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs7134070
rs7134070
1 12 1758235 intron variant T/C snv 5.3E-02 0.700 1.000 1 2012 2012