Variant (rsID / SNP)

rs35629274

rs35629274 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XPC. Location: chromosome 3, position 14,206,353. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

XPCBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 3:14206353
Cytoband: 3p25.1
HGVS: NM_004628.5(XPC):c.860T>G (p.Phe287Cys)
Allele change: Silent

Associated conditions / phenotypes

Xeroderma pigmentosum, group C

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.