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: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.700 1 2016 2016
dbSNP: rs1048943
rs1048943
53 0.572 0.571 15 74720644 missense variant T/C snp 0.11 5.0E-02 0.010 1.000 1 2013 2013
dbSNP: rs1057519747
rs1057519747
17 0.715 0.250 17 7675094 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519757
rs1057519757
5 0.878 0.107 5 68293310 missense variant G/A,C snp 0.700 1 2016 2016
dbSNP: rs1057519828
rs1057519828
1 7 55143387 missense variant G/A snp 0.700 1 2007 2007
dbSNP: rs1057519829
rs1057519829
1 7 55154050 missense variant A/C,G snp 4.0E-06 0.700 1 2007 2007
dbSNP: rs1057519841
rs1057519841
5 0.923 0.107 5 68295269 missense variant A/G snp 0.700 1 2016 2016
dbSNP: rs1057519887
rs1057519887
3 0.923 0.036 7 55154128 missense variant GC/AA,AT multinucleotide-polymorphism 0.700 1 2016 2016
dbSNP: rs1057519888
rs1057519888
3 0.923 0.071 7 55143386 missense variant A/G snp 0.700 1 2016 2016
dbSNP: rs1057519902
rs1057519902
4 0.878 0.107 1 226064451 missense variant G/C snp 0.700 1 2016 2016
dbSNP: rs1057519906
rs1057519906
5 0.878 0.107 15 90088607 missense variant T/A,C snp 0.700 1 2016 2016
dbSNP: rs1057519925
rs1057519925
10 0.769 0.179 3 179210291 missense variant G/A,C snp 0.700 1 2016 2016
dbSNP: rs1057519926
rs1057519926
10 0.769 0.179 3 179210293 missense variant A/T snp 0.700 1 2016 2016
dbSNP: rs1057519927
rs1057519927
16 0.724 0.179 3 179218295 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519932
rs1057519932
21 0.679 0.286 3 179234298 missense variant T/G snp 0.700 1 2016 2016
dbSNP: rs1057519933
rs1057519933
10 0.801 0.250 3 179199156 missense variant A/G snp 0.700 1 2016 2016
dbSNP: rs1057519934
rs1057519934
10 0.801 0.250 3 179199158 missense variant G/C snp 0.700 1 2016 2016
dbSNP: rs1057519935
rs1057519935
10 0.801 0.250 3 179199157 missense variant A/G snp 0.700 1 2016 2016
dbSNP: rs1057519936
rs1057519936
11 0.769 0.179 3 179234284 missense variant A/G,T snp 0.700 1 2016 2016
dbSNP: rs1057519937
rs1057519937
11 0.769 0.179 3 179234285 missense variant T/C snp 0.700 1 2016 2016
dbSNP: rs1057519940
rs1057519940
12 0.756 0.179 3 179218308 missense variant G/T snp 0.700 1 2016 2016
dbSNP: rs1057519975
rs1057519975
13 0.744 0.214 17 7675209 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519978
rs1057519978
12 0.756 0.321 17 7675191 missense variant A/C,G,T snp 0.700 1 2016 2016
dbSNP: rs1057519981
rs1057519981
17 0.715 0.321 17 7674251 stop lost A/C,G snp 0.700 1 2016 2016
dbSNP: rs1057519983
rs1057519983
16 0.715 0.357 17 7673797 missense variant A/G snp 0.700 1 2016 2016