RS558269137 FLG

Health Risk Chr 1:152312601
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What This Variant Does
"rs558269137, also known as c.2284del4, c.2284delAGCT and c.2282_2285delCAGT, is a mutation in the FL...
Associated Conditions
Ichthyosis vulgaris
Dermatitis
atopic
2
susceptibility to
Eczematoid dermatitis
FLG-related disorder
Autosomal dominant ichthyosis vulgaris
Inborn genetic diseases
Autosomal recessive congenital ichthyosis
Palmoplantar keratodermas
Ichthyosis and erythrokeratoderma
Autosomal recessive nonsyndromic hearing loss 1A
Ichthyosis vulgaris
Dermatitis
GWAS Studies (5)
Trait Risk Allele OR / Beta P-value Study
Atopic dermatitis — OR: 0.69 5E-72 PubMed
Atopic dermatitis — OR: 0.64 2E-61 PubMed
Atopic dermatitis CACTG β: 0.5 3E-44 PubMed
Asthma C OR: 0.29 7E-23 PubMed
Atopic dermatitis C OR: 1.03 1E-18 PubMed
Other Variants in FLG
rs61816761 rs121909626 rs41370446 rs150597413 rs397507563 rs138726443 rs146466242 rs797045090 rs147145234 rs761212672
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