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Variant (rsID / SNP)

rs12637558

ATP13A5

rs12637558 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP13A5. Location: chromosome 3, position 193,081,122. The table records no clinical significance for this variant.

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Reference-table entries

ATP13A5Not classified
Variant type
missense_variant
Chromosome / position
3:193081122
HGVS
NM_198505.4,c.287C>A,p.Ser96Tyr
Allele change
Missense_S96Y

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.