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: rs13196329
rs13196329
2 0.925 0.120 6 32357594 intron variant A/C snv 2.6E-02 0.710 1.000 1 2017 2017
dbSNP: rs1633096
rs1633096
1 1.000 0.120 6 29739490 intron variant G/T snv 0.24 0.710 1.000 1 2017 2017
dbSNP: rs9269081
rs9269081
4 0.851 0.280 6 32473323 intron variant A/C snv 0.69 0.010 1.000 1 2017 2017