Variant (rsID / SNP)

rs117444825

rs117444825 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A5. Location: chromosome 7, position 103,033,496. Clinical significance in the table: Benign.

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Reference-table entries

SLC26A5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:103033496
Cytoband: 7q22.1
HGVS: NM_198999.3(SLC26A5):c.989A>G (p.Asn330Ser)
Allele change: Missense_N330S

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.