rs2066853, AHR

N. diseases: 34
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2002 2002
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2002 2002
Colonic Polyps
CUI: C0009376
Disease: Colonic Polyps
8 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2018 2018
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
232 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Glioma
CUI: C0017638
Disease: Glioma
353 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2012 2012
Healthcare associated pneumonia
CUI: C1443237
Disease: Healthcare associated pneumonia
2 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2014 2014
Hospital acquired pneumonia
CUI: C0949083
Disease: Hospital acquired pneumonia
2 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2014 2014
Hyperlipidemia
CUI: C0020473
Disease: Hyperlipidemia
83 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2015 2015
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2016 2016
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2002 2002
Micropenis
CUI: C4551492
Disease: Micropenis
21 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2005 2005
Penis agenesis
CUI: C1387005
Disease: Penis agenesis
11 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2005 2005
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Respiratory Distress Syndrome, Adult
CUI: C0035222
Disease: Respiratory Distress Syndrome, Adult
60 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2017 2017
Sessile Serrated Adenoma/Polyp
CUI: C2732618
Disease: Sessile Serrated Adenoma/Polyp
6 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Severe dry skin
CUI: C3839047
Disease: Severe dry skin
2 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2019 2019
Tumor Cell Invasion
CUI: C1269955
Disease: Tumor Cell Invasion
169 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2014 2014
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2012 2012
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2012 2012
Xeroderma Pigmentosum, Complementation Group D
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
111 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.010 1.000 1 2004 2004
Acromegaly
CUI: C0001206
Disease: Acromegaly
25 0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 0.020 1.000 2 2014 2019