Variant (rsID / SNP)

rs751402

rs751402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERCC5. Location: chromosome 13, position 103,498,198. Clinical significance in the table: Benign.

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Reference-table entries

ERCC5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:103498198
Cytoband: 13q33.1
HGVS: NM_000123.3(ERCC5):c.-419A>G
Allele change: Silent

Associated conditions / phenotypes

Xeroderma pigmentosum, group G

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.