Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs118204117
rs118204117
1.000 0.160 11 119092958 stop gained G/A;C snv 1.2E-05
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.730 1.000 0 1994 2001
dbSNP: rs118204119
rs118204119
1.000 0.160 11 119089248 missense variant T/C snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs118204120
rs118204120
1.000 0.160 11 119090212 stop gained C/T snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1205219549
rs1205219549
1.000 0.160 11 119092156 missense variant T/A snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.710 1.000 20 1991 2015
dbSNP: rs1261947877
rs1261947877
1.000 0.160 11 119092416 missense variant G/A;T snv 1.2E-05; 4.0E-06
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.710 1.000 0 1998 1998
dbSNP: rs1334178100
rs1334178100
1.000 0.160 11 119092768 missense variant G/A snv 7.0E-06
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs142459647
rs142459647
1.000 0.160 11 119092426 missense variant G/A snv 1.7E-04 2.2E-04
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 1.000 20 1991 2015
dbSNP: rs150763621
rs150763621
1.000 0.160 11 119089263 stop gained A/T snv 8.3E-04 5.0E-04
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 1.000 20 1991 2015
dbSNP: rs1555206128
rs1555206128
1.000 0.160 11 119092417 inframe deletion AGTGCGAGCCAAGGACCAGGACATCTTGGA/- delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1555206402
rs1555206402
0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565754285
rs1565754285
1.000 0.160 11 119089094 frameshift variant C/- delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565754296
rs1565754296
1.000 0.160 11 119089098 frameshift variant -/G delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565754452
rs1565754452
1.000 0.160 11 119089216 splice acceptor variant G/A snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565754565
rs1565754565
1.000 0.160 11 119089273 splice donor variant G/C snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565756481
rs1565756481
1.000 0.160 11 119091412 splice acceptor variant G/A snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565757839
rs1565757839
1.000 0.160 11 119092480 frameshift variant CT/- delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565757857
rs1565757857
1.000 0.160 11 119092481 frameshift variant -/TTCGCTGC delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565758008
rs1565758008
1.000 0.160 11 119092524 splice donor variant G/C snv
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565758795
rs1565758795
1.000 0.160 11 119092999 frameshift variant -/T delins
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs1565758825
rs1565758825
1.000 0.160 11 119093009 frameshift variant T/- del
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs189159450
rs189159450
1.000 0.160 11 119088285 missense variant C/G;T snv 4.0E-06; 1.6E-05 2.1E-05
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs34413634
rs34413634
1.000 0.160 11 119091497 missense variant C/T snv 6.4E-06 7.0E-06
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.700 0
dbSNP: rs536814318
rs536814318
1.000 0.160 11 119091446 missense variant G/A snv 5.0E-04 2.8E-05
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.810 1.000 20 1991 2015
dbSNP: rs575222284
rs575222284
1.000 0.160 11 119091431 missense variant C/T snv 1.3E-05 7.0E-06
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.730 1.000 0 1997 2006
dbSNP: rs761004837
rs761004837
1.000 0.160 11 119089097 missense variant C/T snv 1.1E-04 4.9E-05
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
0.710 1.000 0 2008 2008