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Variant (rsID / SNP)

rs113498662

ADGRV1

rs113498662 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRV1. Location: chromosome 5, position 90,049,470. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ADGRV1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:90049470
Cytoband
5q14.3
HGVS
NM_032119.4(ADGRV1):c.11201T>C (p.Val3734Ala)
Allele change
Missense_V3734A

Associated conditions / phenotypes

Usher syndrome type 2C

Public references

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