rs1801144

This variant is located in the ROM1 gene.

GWAS Catalog Trait Associations (3)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

forced expiratory volume

Allele C
OR 0.02
p 2.0e-28
N 394,642
Large GWAS
European
Allele C
OR 0.01
p 1.0e-12
N 373,397
Large GWAS
European

vital capacity

Allele C
OR 0.02
p 1.0e-23
N 394,642
Large GWAS
European

forced expiratory volume, 25-hydroxyvitamin D3 measurement

Allele G
OR
p 8.0e-10
N 115,312
Meta-analysisLarge GWAS
multi-ancestry

ClinVar annotation

Benign★★★
5 submitters2 publications

Retinitis pigmentosa; not provided; Retinal dystrophy

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About ROM1

This gene is a member of a photoreceptor-specific gene family and encodes an integral membrane protein found in the photoreceptor disk rim of the eye. This protein can form homodimers or can heterodimerize with another photoreceptor, retinal degeneration slow (RDS). It is essential for disk morphogenesis, and may also function as an adhesion molecule involved in the stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa. [provided by RefSeq, Jul 2008]

View all ROM1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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