Gene: INHCAP ×
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: rs10935073
rs10935073
TF ; INHCAP
1 3 133720340 intron variant T/C snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs11921527
rs11921527
TF ; INHCAP
1 3 133722323 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs12639304
rs12639304
TF ; INHCAP
1 3 133722750 intron variant A/T snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs1800277
rs1800277
TF ; INHCAP
1 3 133747311 intron variant C/T snv 7.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs4459901
rs4459901
TF ; INHCAP
1 3 133746855 intron variant T/C snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs4525863
rs4525863
TF ; INHCAP
2 1.000 0.080 3 133717292 intron variant C/A snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs6439431
rs6439431
TF ; INHCAP
1 3 133729265 intron variant A/C snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs6774822
rs6774822
TF ; INHCAP
1 3 133723168 intron variant G/C;T snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs6775042
rs6775042
TF ; INHCAP
1 3 133723401 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs6782523
rs6782523
TF ; INHCAP
1 3 133720073 intron variant C/G;T snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs6785596
rs6785596
TF ; INHCAP
1 3 133747613 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs6787177
rs6787177
TF ; INHCAP
1 3 133731876 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs6796795
rs6796795
TF ; INHCAP
1 3 133747378 intron variant A/G snv 8.0E-02 0.700 1.000 1 2011 2011
dbSNP: rs7646118
rs7646118
TF ; INHCAP
1 3 133731195 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs8177178
rs8177178
TF ; INHCAP
3 0.925 0.080 3 133744428 intron variant G/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs8177191
rs8177191
TF ; INHCAP
1 3 133749295 intron variant G/A snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs8177197
rs8177197
TF ; INHCAP
1 3 133750686 intron variant G/A snv 0.27 0.700 1.000 1 2011 2011
dbSNP: rs8177213
rs8177213
TF ; INHCAP
1 3 133753383 intron variant A/C snv 0.25 0.700 1.000 1 2011 2011
dbSNP: rs8177313
rs8177313
TF ; INHCAP
1 3 133745258 intron variant T/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs9830001
rs9830001
TF ; INHCAP
1 3 133714626 intron variant G/A;C snv 0.700 1.000 1 2011 2011