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: rs17197936
rs17197936
3 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 0.010 1.000 1 2014 2014
dbSNP: rs2295826
rs2295826
4 0.851 0.200 14 52708205 intron variant A/G snv 0.11 0.010 1.000 1 2014 2014
dbSNP: rs2295827
rs2295827
4 0.851 0.200 14 52708263 intron variant C/T snv 9.6E-02 9.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs2348071
rs2348071
5 0.827 0.240 14 58263908 intron variant A/G snv 0.71 0.010 1.000 1 2014 2014