Variant (rsID / SNP)

rs17235409

rs17235409 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC11A1. Location: chromosome 2, position 219,259,732. Clinical significance in the table: risk factor.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC11A1Risk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 2:219259732
Cytoband: 2q35
HGVS: NM_000578.4(SLC11A1):c.1627G>A (p.Asp543Asn)
Allele change: Missense_D543N

Associated conditions / phenotypes

Buruli ulcer, susceptibility to

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.