Variant (rsID / SNP)

rs34407351

rs34407351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC26A3. Location: chromosome 7, position 107,427,322. 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: 7:107427322
Cytoband: 7q22.3
HGVS: NM_000111.3(SLC26A3):c.921T>G (p.Cys307Trp)
Allele change: Missense_C307W

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.