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: rs1800896
rs1800896
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.010 1.000 1 2014 2014
dbSNP: rs1878672
rs1878672
3 0.882 0.080 1 206770368 intron variant G/A;C;T snv 0.010 1.000 1 2014 2014
dbSNP: rs3024491
rs3024491
2 0.925 0.040 1 206771701 intron variant C/A;T snv 0.010 1.000 1 2014 2014