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Variant (rsID / SNP)

rs1799802

ERCC4

rs1799802 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERCC4. Location: chromosome 16, position 14,028,081. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ERCC4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:14028081
Cytoband
16p13.12
HGVS
NM_005236.3(ERCC4):c.1135C>T (p.Pro379Ser)
Allele change
Missense_P379S

Associated conditions / phenotypes

Fanconi anemia complementation group Q|Xeroderma pigmentosum, group F|Cockayne syndrome|Xeroderma pigmentosum, group F|Xeroderma pigmentosum

Public references

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