Source: ALL

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: rs10264856
rs10264856
ABCB1 ; RUNDC3B
7 87633265 intron variant G/A snv 0.16
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2015 2015
dbSNP: rs17327624
rs17327624
ABCB1
7 87587501 intron variant G/A;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2016 2016
dbSNP: rs200748388
rs200748388
ABCB1
7 87601021 5 prime UTR variant G/A snv 7.0E-06
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.010 1.000 1 2015 2015
dbSNP: rs4148734
rs4148734
ABCB1
7 87564281 intron variant G/A snv 0.22
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2016 2016
dbSNP: rs56364292
rs56364292
ABCB1
7 87558776 intron variant C/T snv 0.10
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs745614189
rs745614189
ABCB1
7 87549387 synonymous variant G/A snv 4.0E-06
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.010 1.000 1 2015 2015
dbSNP: rs1128501
rs1128501
ABCB1
7 87566218 missense variant C/A snv
CUI: C1861502
Disease: COLCHICINE RESISTANCE
COLCHICINE RESISTANCE 		0.700 0
dbSNP: rs10234411
rs10234411
ABCB1
1.000 0.040 7 87535576 intron variant T/A;C;G snv
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.010 1.000 1 2015 2015
dbSNP: rs10276036
rs10276036
ABCB1
1.000 0.040 7 87550882 intron variant C/A;T snv 1.2E-05; 0.53
CUI: C0746883
Disease: Febrile Neutropenia
Febrile Neutropenia 		0.010 1.000 1 2016 2016
dbSNP: rs1202186
rs1202186
ABCB1
1.000 0.040 7 87583942 intron variant C/T snv 0.69
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs12720066
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02
CUI: C0023530
Disease: Leukopenia
Leukopenia 		0.010 1.000 1 2018 2018
dbSNP: rs12720066
rs12720066
ABCB1
0.925 0.040 7 87540386 intron variant A/C snv 3.9E-02
CUI: C0027947
Disease: Neutropenia
Neutropenia 		0.010 1.000 1 2018 2018
dbSNP: rs13233308
rs13233308
ABCB1
1.000 0.040 7 87615644 intron variant C/T snv 0.36
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2015 2015
dbSNP: rs13233308
rs13233308
ABCB1
1.000 0.040 7 87615644 intron variant C/T snv 0.36
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs17327442
rs17327442
ABCB1
1.000 0.040 7 87583674 intron variant T/A snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs200754866
rs200754866
ABCB1
1.000 0.040 7 87536484 missense variant C/A;T snv 1.2E-05; 3.6E-05
CUI: C0023530
Disease: Leukopenia
Leukopenia 		0.010 1.000 1 2009 2009
dbSNP: rs2032583
rs2032583
ABCB1
1.000 0.040 7 87531245 intron variant A/G snv 0.12 0.13
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2019 2019
dbSNP: rs2091766
rs2091766
ABCB1
1.000 0.040 7 87545188 intron variant C/A;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs2235015
rs2235015
ABCB1
1.000 0.040 7 87570248 intron variant C/A;T snv 0.18 0.23
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2019 2019
dbSNP: rs2235035
rs2235035
ABCB1
0.925 0.040 7 87549770 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2004 2004
dbSNP: rs2235035
rs2235035
ABCB1
0.925 0.040 7 87549770 intron variant G/A snv 0.29
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2004 2004
dbSNP: rs2235040
rs2235040
ABCB1
1.000 0.040 7 87536434 intron variant C/A;G;T snv 0.12 0.13
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.010 1.000 1 2019 2019
dbSNP: rs2235046
rs2235046
ABCB1
0.925 0.040 7 87544750 intron variant T/A;C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 1.000 1 2009 2009
dbSNP: rs2235046
rs2235046
ABCB1
0.925 0.040 7 87544750 intron variant T/A;C;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2009 2009
dbSNP: rs3747802
rs3747802
ABCB1 ; RUNDC3B
1.000 0.040 7 87713270 5 prime UTR variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2019 2019