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: rs12373124
rs12373124
9 0.790 0.120 17 45846853 synonymous variant T/C snv 0.15 0.14 0.700 1.000 1 2017 2017
dbSNP: rs140843301
rs140843301
1 1.000 0.080 17 45861848 intron variant T/C;G snv 0.700 1.000 1 2017 2017
dbSNP: rs143942024
rs143942024
1 1.000 0.080 17 45849092 intron variant C/A;T snv 1.1E-02 0.700 1.000 1 2017 2017