Variant (rsID / SNP)

rs1800975

rs1800975 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to XPA. Location: chromosome 9, position 100,459,578. Clinical significance in the table: Benign.

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Reference-table entries

XPABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:100459578
Cytoband: 9q22.33
HGVS: NM_000380.4(XPA):c.-4A>G
Allele change: Silent

Associated conditions / phenotypes

Xeroderma pigmentosum group A

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.