Variant (rsID / SNP)

rs6427504

rs6427504 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP1A4. Location: chromosome 1, position 160,124,875. The table records no clinical significance for this variant.

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Reference-table entries

ATP1A4Not classified

Variant type: missense_variant
Chromosome / position: 1:160124875
HGVS: NM_144699.4,c.248G>A,p.Gly83Asp
Allele change: Missense_G83D

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.