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: rs2696625
rs2696625
1 17 46249498 downstream gene variant A/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs2764261
rs2764261
3 6 108606639 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2854277
rs2854277
1 6 32660307 intron variant C/T snv 0.700 1.000 1 2018 2018
dbSNP: rs2988004
rs2988004
1 9 37044391 upstream gene variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs3094622
rs3094622
1 6 30360175 upstream gene variant A/G snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs3101340
rs3101340
1 1 72278461 intron variant G/A snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs328902
rs328902
1 7 34981231 intron variant C/T snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs34858520
rs34858520
1 7 72258898 intron variant A/G snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs3781411
rs3781411
1 10 125026867 missense variant C/T snv 0.15 0.14 0.700 1.000 1 2018 2018
dbSNP: rs429358
rs429358
66 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 0.700 1.000 1 2018 2018
dbSNP: rs4576826
rs4576826
1 11 66793511 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs4865656
rs4865656
1 5 51363954 intergenic variant G/A snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs55872725
rs55872725
FTO
6 16 53775211 intron variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs564819152
rs564819152
1 10 21531721 intron variant A/G snv 0.700 1.000 1 2018 2018
dbSNP: rs61776614
rs61776614
SKI
1 1 2234967 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs62253088
rs62253088
1 3 85351651 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs62398709
rs62398709
1 5 152675675 intron variant A/T snv 0.34 0.700 1.000 1 2018 2018
dbSNP: rs6433478
rs6433478
1 2 174376754 intron variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs6689056
rs6689056
1 1 24038041 upstream gene variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs6775319
rs6775319
1 3 18717009 intron variant A/T snv 0.76 0.700 1.000 1 2018 2018
dbSNP: rs6870096
rs6870096
1 5 152566250 intron variant C/G snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs6895232
rs6895232
1 5 152659861 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7548269
rs7548269
1 1 20762979 intron variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs75930676
rs75930676
1 14 71359830 intron variant T/C snv 3.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs7791992
rs7791992
1 7 50198188 downstream gene variant C/A;T snv 0.700 1.000 1 2018 2018