Variant (rsID / SNP)

rs10929303

rs10929303 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COVERS 10 GENES, covers 10 genes. Location: chromosome 2, position 234,681,416. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

COVERS 10 GENESBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:234681416
Cytoband: 2q37.1
HGVS: NM_000463.3(UGT1A1):c.*211T>C
Allele change: Silent

Associated conditions / phenotypes

Gilbert syndrome|Crigler-Najjar syndrome|Lucey-Driscoll syndrome

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.