Variant (rsID / SNP)

rs16883930

rs16883930 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC17A5. Location: chromosome 6, position 74,331,619. Clinical significance in the table: Benign/Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC17A5Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:74331619
Cytoband: 6q13
HGVS: NM_012434.5(SLC17A5):c.886G>A (p.Val296Ile)
Allele change: Missense_V296I

Associated conditions / phenotypes

Salla disease|Sialic acid storage disease, severe infantile 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.