rs2066845, NOD2

N. diseases: 5
Source: GWASCAT ×
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
544 0.662 0.429 16 50722629 missense variant G/C,T snp 1.1E-02; 2.2E-04 7.8E-03; 3.2E-05 1.000 0.933 1 2002 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
452 0.662 0.429 16 50722629 missense variant G/C,T snp 1.1E-02; 2.2E-04 7.8E-03; 3.2E-05 0.880 0.500 1 2002 2017
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
331 0.662 0.429 16 50722629 missense variant G/C,T snp 1.1E-02; 2.2E-04 7.8E-03; 3.2E-05 0.720 0.500 1 2002 2017
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
265 0.662 0.429 16 50722629 missense variant G/C,T snp 1.1E-02; 2.2E-04 7.8E-03; 3.2E-05 0.700 1 2017 2017
Psoriasis
CUI: C0033860
Disease: Psoriasis
449 0.662 0.429 16 50722629 missense variant G/C,T snp 1.1E-02; 2.2E-04 7.8E-03; 3.2E-05 0.700 1 2017 2017