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: rs1017226
rs1017226
2 0.925 0.080 5 56857565 intron variant T/C snv 5.8E-02 0.710 1.000 2 2014 2016
dbSNP: rs16886364
rs16886364
2 0.925 0.080 5 56826517 intron variant A/G snv 5.8E-02 0.710 1.000 2 2014 2016
dbSNP: rs16886397
rs16886397
4 0.925 0.080 5 56838449 intron variant A/G snv 5.8E-02 0.710 1.000 2 2014 2016
dbSNP: rs16886448
rs16886448
3 0.882 0.080 5 56874986 intron variant C/G snv 6.6E-02 5.8E-02 0.710 1.000 2 2014 2016
dbSNP: rs2229882
rs2229882
2 0.925 0.080 5 56872885 synonymous variant C/T snv 4.8E-02 4.4E-02 0.710 1.000 2 2014 2016
dbSNP: rs3822625
rs3822625
1 1.000 0.080 5 56882284 synonymous variant A/G snv 7.2E-02 7.8E-02 0.700 1.000 1 2014 2014