Variant (rsID / SNP)

rs116900495

rs116900495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A5. Location: chromosome 7, position 103,062,016. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLC26A5Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:103062016
Cytoband: 7q22.1
HGVS: NM_198999.3(SLC26A5):c.-53-2A>G
Allele change: Silent

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 61

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.