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: rs10157710
rs10157710 		1 1 47496019 downstream gene variant C/T snv 0.78 0.700 1.000 1 2018 2018
dbSNP: rs112607182
rs112607182 		2 3 170309619 downstream gene variant C/T snv 5.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs11264327
rs11264327 		1 1 155122631 downstream gene variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12032996
rs12032996 		1 1 33454985 intergenic variant G/A snv 0.12 0.700 1.000 1 2018 2018
dbSNP: rs12727104
rs12727104 		1 1 171454028 intergenic variant G/A snv 8.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs13394343
rs13394343 		1 2 85527219 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs16943246
rs16943246 		1 15 45428399 upstream gene variant G/A snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs17158386
rs17158386 		2 7 29765745 regulatory region variant G/A snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs185291443
rs185291443 		1 2 226120788 intergenic variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs2472297
rs2472297 		9 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		13 1.000 0.040 8 125487789 intron variant C/G snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs35311980
rs35311980 		1 2 228295484 intergenic variant C/T snv 4.9E-05 0.700 1.000 1 2019 2019
dbSNP: rs35924503
rs35924503 		1 2 228266570 intergenic variant T/C snv 1.5E-04 0.700 1.000 1 2018 2018
dbSNP: rs4288924
rs4288924 		1 14 68835682 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6712846
rs6712846 		1 2 207024356 intergenic variant G/A snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs10995311
rs10995311
ADO
3 10 62805174 missense variant C/G snv 0.35 0.31 0.700 1.000 1 2018 2018
dbSNP: rs2236295
rs2236295
ADO
2 10 62805132 missense variant G/C;T snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs4410790
rs4410790
AHR ; LOC101927609
9 0.882 0.160 7 17244953 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs11162351
rs11162351
AK5
1 1 77479047 intron variant C/G snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs144994089
rs144994089
AQP7
1 9 33385158 missense variant C/T snv 7.0E-04 8.2E-04 0.700 1.000 1 2018 2018
dbSNP: rs702634
rs702634
ARL15
3 1.000 0.080 5 53975590 intron variant G/A snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs35572189
rs35572189
BAHCC1 ; MIR3186
1 17 81451999 missense variant G/A;C snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs34823645
rs34823645
C2orf83
1 2 227647210 intron variant T/C snv 3.9E-04 0.700 1.000 1 2019 2019
dbSNP: rs2601006
rs2601006
CCT2 ; MIR3913-1
1 12 69585737 5 prime UTR variant C/T snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs4738817
rs4738817
CHD7
1 8 60708054 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018