RS35667974 Unknown gene

Other Chr 2:162268127
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What This Variant Does
"rs35667974, also known as Ile923Val, is a SNP in the interferon induced with helicase C domain 1 IFI..."
GWAS Studies (15)
Trait Risk Allele OR / Beta P-value Study
IFNL1 protein levels C OR: 0.32 9E-53 PubMed
Hypothyroidism C OR: 0.18 1E-38 PubMed
Lymphocyte count C 4E-15 PubMed
Hypothyroidism C OR: 0.28 3E-14 PubMed
X-12127 levels T OR: 0.25 6E-13 PubMed
Autoimmune thyroid disease T OR: 1.27 9E-13 PubMed
Type 1 diabetes OR: 1.9 1E-11 PubMed
ICD10 L43: Lichen planus OR: 0.37 2E-10 PubMed
Lymphoid neoplasms OR: 1.21 4E-10 PubMed
Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) 5E-10 PubMed
Type 1 diabetes T OR: 1.69 9E-9 PubMed
Lymphoid neoplasms (B-cell phenocluster) OR: 1.32 4E-8 PubMed
Lymphoid neoplasms (somatic mutation group 1 phenocluster) OR: 1.62 4E-7 PubMed
Oral lichen planus OR: 0.48 4E-6 PubMed
Autoimmune thyroid disease C OR: 0.85 4E-6 PubMed
Ask Dr. Hemsworth about this variant