Variant (rsID / SNP)

rs35761929

rs35761929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JAG1. Location: chromosome 20, position 10,622,501. Clinical significance in the table: Benign.

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Reference-table entries

JAG1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 20:10622501
Cytoband: 20p12.2
HGVS: NM_000214.3(JAG1):c.2612C>G (p.Pro871Arg)
Allele change: Missense_P871R

Associated conditions / phenotypes

Cardiovascular phenotype|Isolated Nonsyndromic Congenital Heart Disease|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.