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: rs12473379
rs12473379
1 1.000 0.040 2 176581595 intron variant C/G snv 0.44 0.700 1.000 1 2012 2012
dbSNP: rs1448522
rs1448522
1 1.000 0.040 2 176577912 intron variant G/A snv 0.54 0.700 1.000 1 2012 2012
dbSNP: rs2922346
rs2922346
1 1.000 0.040 2 176580981 intron variant A/G snv 0.55 0.700 1.000 1 2012 2012