Variant (rsID / SNP)

rs57655409

rs57655409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRXCR1. Location: chromosome 4, position 42,895,423. Clinical significance in the table: Benign.

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Reference-table entries

GRXCR1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:42895423
Cytoband: 4p13
HGVS: NM_001080476.3(GRXCR1):c.140C>T (p.Ala47Val)
Allele change: Missense_A47V

Associated conditions / phenotypes

Autosomal recessive nonsyndromic hearing loss 25

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.