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Variant (rsID / SNP)

rs148095899

ERCC6

rs148095899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ERCC6. Location: chromosome 10, position 50,740,611. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

ERCC6Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
10:50740611
Cytoband
10q11.23
HGVS
NM_000124.4(ERCC6):c.400C>T (p.Arg134Trp)
Allele change
Missense_R134W

Associated conditions / phenotypes

Macular degeneration|COFS syndrome|Cockayne syndrome

Public references

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