Variant (rsID / SNP)

rs35885438

rs35885438 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C1QTNF5, MFRP. Location: chromosome 11, position 119,215,046. 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: 11:119215046
Cytoband: 11q23.3
HGVS: NM_031433.4(MFRP):c.954G>A (p.Leu318_Gln319=)
Allele change: Synonymous_L318L

Associated conditions / phenotypes

Retinal degeneration|Isolated microphthalmia 6|Isolated microphthalmia 5

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.