Variant (rsID / SNP)

rs4639950

rs4639950 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1QTNF5, MFRP. Location: chromosome 11, position 119,216,555. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

C1QTNF5Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:119216555
Cytoband: 11q23.3
HGVS: NM_031433.4(MFRP):c.355A>G (p.Ile119Val)
Allele change: Missense_I119V

Associated conditions / phenotypes

Retinal degeneration|Isolated microphthalmia 5|Late-onset retinal degeneration

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.