Source: ALL
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: rs10945918
rs10945918
LOC107986666
1 6 163756289 intron variant C/T snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs6902153
rs6902153
LOC107986666
1 6 163755424 intron variant C/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs6928576
rs6928576
LOC107986666
1 6 163755234 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7149926
rs7149926 		1 14 68864011 downstream gene variant C/T snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs9028
rs9028
RTP4
1 3 187371509 3 prime UTR variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs9736016
rs9736016 		2 1.000 0.080 11 118854185 intergenic variant T/A snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs2237892
rs2237892
KCNQ1
16 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs2237897
rs2237897
KCNQ1
6 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.010 1.000 1 2016 2016