Variant (rsID / SNP)

rs2491014

rs2491014 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP11C. The table records no clinical significance for this variant.

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Reference-table entries

ATP11CNot classified

Variant type: missense_variant
HGVS: NM_173694.5,c.342T>G,p.Cys114Trp
Allele change: Missense_C114W

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.