Variant (rsID / SNP)

rs146547672

rs146547672 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A5. Location: chromosome 7, position 103,018,979. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC26A5Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:103018979
Cytoband: 7q22.1
HGVS: NM_198999.3(SLC26A5):c.1699A>G (p.Ile567Val)
Allele change: Missense_I567V

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.