Source: BEFREE ×
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: rs1129293
rs1129293
3 0.882 0.040 7 106872566 synonymous variant C/T snv 0.32 0.26 0.010 1.000 1 2018 2018
dbSNP: rs17847825
rs17847825
1 1.000 7 106868886 missense variant C/A;T snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs2230460
rs2230460
2 0.925 0.040 7 106884244 synonymous variant C/T snv 0.12 8.5E-02 0.010 1.000 1 2018 2018