Variant (rsID / SNP)

rs145877051

rs145877051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC34A3. Location: chromosome 9, position 140,127,809. Clinical significance in the table: Likely benign.

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Reference-table entries

SLC34A3Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:140127809
Cytoband: 9q34.3
HGVS: NM_001177316.2(SLC34A3):c.709G>A (p.Asp237Asn)
Allele change: Missense_D237N

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.