Variant (rsID / SNP)

rs61731389

rs61731389 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCDH15. Location: chromosome 10, position 55,892,642. Clinical significance in the table: Benign.

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Reference-table entries

PCDH15Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:55892642
Cytoband: 10q21.1
HGVS: NM_001384140.1(PCDH15):c.1910A>G (p.Asn637Ser)
Allele change: Missense_N637S

Associated conditions / phenotypes

Usher syndrome type 1|Usher syndrome type 1F|Autosomal recessive nonsyndromic hearing loss 23

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.