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Variant (rsID / SNP)

rs370454709

ERCC2

rs370454709 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERCC2. Location: chromosome 19, position 45,867,532. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ERCC2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:45867532
Cytoband
19q13.32
HGVS
NM_000400.4(ERCC2):c.776G>A (p.Cys259Tyr)
Allele change
Missense_C259Y

Associated conditions / phenotypes

ERCC2-Related Disorders|Xeroderma pigmentosum

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.