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: rs3730051
rs3730051
1 1.000 0.120 19 40238790 intron variant T/C snv 0.24 0.010 1.000 1 2008 2008
dbSNP: rs8100018
rs8100018
1 1.000 0.120 19 40246116 intron variant C/A;G snv 0.010 1.000 1 2008 2008