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: rs1333049
rs1333049
60 0.614 0.520 9 22125504 intron variant G/C snv 0.41 0.010 1.000 1 2015 2015
dbSNP: rs1537370
rs1537370
2 1.000 9 22084311 intron variant C/T snv 0.55 0.010 1.000 1 2015 2015
dbSNP: rs2026458
rs2026458
6 0.882 0.080 6 12825642 intron variant C/T snv 0.34 0.010 1.000 1 2015 2015