Variant (rsID / SNP)

rs2237964

rs2237964 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USH1C. Location: chromosome 11, position 17,532,102. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

USH1CBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:17532102
Cytoband: 11p15.1
HGVS: NM_153676.4(USH1C):c.1414-34G>A
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 18A|Usher syndrome type 1C

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.