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Variant (rsID / SNP)

rs77332724

ATP1A4

rs77332724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP1A4. Location: chromosome 1, position 160,121,899. The table records no clinical significance for this variant.

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Reference-table entries

ATP1A4Not classified
Variant type
synonymous_variant
Chromosome / position
1:160121899
HGVS
NM_144699.4,c.69A>G,p.Lys23Lys
Allele change
Synonymous_K23K

Public references

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