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: rs11677607
rs11677607
1 2 100134688 intron variant C/T snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs73966422
rs73966422
1 2 100137627 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs72755233
rs72755233
5 1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 0.700 1.000 1 2019 2019
dbSNP: rs400301
rs400301
1 3 10015782 intron variant G/A snv 6.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs57989773
rs57989773
2 1.000 0.080 6 100181202 downstream gene variant T/C snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs13002946
rs13002946
1 2 100185497 intron variant T/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs6542924
rs6542924
1 2 100276651 3 prime UTR variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs4851287
rs4851287
1 2 100299310 missense variant A/G snv 0.69 0.72 0.700 1.000 1 2018 2018
dbSNP: rs9299338
rs9299338
1 9 100345896 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs17094222
rs17094222
3 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 0.700 1.000 5 2015 2019
dbSNP: rs2495707
rs2495707
1 10 100666192 downstream gene variant A/G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs12147845
rs12147845
1 14 100678259 intron variant C/T snv 0.10 0.700 1.000 2 2019 2019
dbSNP: rs180963
rs180963
1 6 100679337 intron variant T/C snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs41310284
rs41310284
3 10 100687890 intergenic variant C/A;T snv 0.700 1.000 2 2019 2019
dbSNP: rs6907240
rs6907240
1 6 100705906 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs12209887
rs12209887
1 6 100708930 intron variant G/A snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs34277166
rs34277166
1 10 100875096 regulatory region variant G/A snv 0.40 0.700 1.000 1 2019 2019
dbSNP: rs1799805
rs1799805
1 7 100893176 missense variant G/T snv 4.0E-02 3.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs10883560
rs10883560
1 10 100913950 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3134353
rs3134353
1 8 100935225 intron variant A/C;G;T snv 0.700 1.000 2 2015 2018
dbSNP: rs3134358
rs3134358
1 8 100946205 intron variant G/T snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs7817485
rs7817485
1 8 100957300 upstream gene variant T/C;G snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs7161194
rs7161194
2 14 101062668 upstream gene variant A/G;T snv 0.700 1.000 2 2018 2019
dbSNP: rs7147503
rs7147503
1 14 101073047 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs12431682
rs12431682
1 14 101073662 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019