Variant (rsID / SNP)

rs3735605

rs3735605 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A3. Location: chromosome 7, position 107,423,254. Clinical significance in the table: Benign.

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Reference-table entries

SLC26A3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 7:107423254
Cytoband: 7q22.3
HGVS: NM_000111.3(SLC26A3):c.1299G>A (p.Ala433=)
Allele change: Synonymous_A433A

Associated conditions / phenotypes

Congenital secretory diarrhea, chloride type

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.