Gene: ANK3 ×
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: rs12412135
rs12412135
ANK3
1 1.000 0.040 10 60523076 intron variant C/T snv 9.2E-02 0.700 1.000 1 2014 2014
dbSNP: rs12416380
rs12416380
ANK3
1 1.000 0.040 10 60396396 intron variant A/G snv 9.5E-02 0.700 1.000 1 2014 2014
dbSNP: rs1380459
rs1380459
ANK3
1 1.000 0.040 10 60337573 intron variant C/T snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs139972937
rs139972937
ANK3
1 1.000 0.040 10 60072953 missense variant T/C snv 2.4E-04 3.8E-04 0.010 1.000 1 2014 2014
dbSNP: rs16915196
rs16915196
ANK3
1 1.000 0.040 10 60600101 intron variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs16915231
rs16915231
ANK3
1 1.000 0.040 10 60615288 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1938540
rs1938540
ANK3
1 1.000 0.040 10 60535056 intron variant C/T snv 8.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs2154393
rs2154393
ANK3
1 1.000 0.040 10 60566929 intron variant C/T snv 8.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs372922084
rs372922084
ANK3
1 1.000 0.040 10 60074916 missense variant A/G snv 1.6E-05 1.4E-05 0.010 1.000 1 2018 2018
dbSNP: rs3808943
rs3808943
ANK3
2 0.925 0.040 10 60391257 intron variant C/T snv 9.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs4948412
rs4948412
ANK3
1 1.000 0.040 10 60386818 intron variant T/C snv 7.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs4948417
rs4948417
ANK3
1 1.000 0.040 10 60401860 intron variant A/G snv 9.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs9633553
rs9633553
ANK3 ; LOC107984292
1 1.000 0.040 10 60514979 intron variant T/G snv 8.3E-02 0.700 1.000 1 2014 2014