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: rs12686004
rs12686004
5 1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1799777
rs1799777
1 9 104903754 5 prime UTR variant -/C delins 0.10 0.700 1.000 1 2018 2018
dbSNP: rs1800978
rs1800978
6 1.000 0.040 9 104903697 5 prime UTR variant C/A;G;T snv 5.4E-06; 0.14 0.700 1.000 1 2018 2018
dbSNP: rs1883025
rs1883025
6 0.807 0.120 9 104902020 intron variant C/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs2575876
rs2575876
6 9 104903458 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs2740488
rs2740488
9 0.827 0.120 9 104899461 intron variant A/C snv 0.29 0.700 1.000 1 2018 2018