Variant (rsID / SNP)

rs111033429

rs111033429 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRV1. Location: chromosome 5, position 89,989,752. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ADGRV1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 5:89989752
Cytoband: 5q14.3
HGVS: NM_032119.4(ADGRV1):c.7179C>T (p.Asp2393=)
Allele change: Synonymous_D2393D

Associated conditions / phenotypes

Usher syndrome type 2C

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.