Variant (rsID / SNP)

rs876660980

rs876660980 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JAG1. Location: chromosome 20, position 10,637,098. Clinical significance in the table: Pathogenic.

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Reference-table entries

JAG1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 20:10637098
Cytoband: 20p12.2
HGVS: NM_000214.3(JAG1):c.703C>T (p.Arg235Ter)
Allele change: Nonsense_R235X

Associated conditions / phenotypes

Alagille syndrome due to a JAG1 point mutation

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.