Variant (rsID / SNP)

rs77319279

rs77319279 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC34A2. Location: chromosome 4, position 25,669,530. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC34A2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:25669530
Cytoband: 4p15.2
HGVS: NM_006424.3(SLC34A2):c.552T>C (p.Ile184=)
Allele change: Synonymous_I184I

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.