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Variant (rsID / SNP)

rs754912569

ATP8B1

rs754912569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ATP8B1. Location: chromosome 18, position 55,315,780. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ATP8B1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
18:55315780
Cytoband
18q21.31
HGVS
NM_001374385.1(ATP8B1):c.3696G>A (p.Ser1232=)
Allele change
Silent

Associated conditions / phenotypes

Progressive familial intrahepatic cholestasis type 1

Public references

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