Variant (rsID / SNP)

rs58757394

rs58757394 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A11. Location: chromosome 20, position 3,209,012. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLC4A11Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:3209012
Cytoband: 20p13
HGVS: NM_001174089.2(SLC4A11):c.2451G>A (p.Thr817=)
Allele change: Synonymous_T817T

Associated conditions / phenotypes

Corneal dystrophy|Corneal dystrophy-perceptive deafness syndrome

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.