Variant (rsID / SNP)

rs6788448

rs6788448 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP13A4. Location: chromosome 3, position 193,209,178. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ATP13A4Not classified

Variant type: missense_variant
Chromosome / position: 3:193209178
HGVS: NM_032279.4,c.543A>G,p.Ile181Met
Allele change: Missense_I181M

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.