Variant (rsID / SNP)

rs376877866

rs376877866 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLX4. Location: chromosome 16, position 3,640,795. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

SLX4Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 16:3640795
Cytoband: 16p13.3
HGVS: NM_032444.4(SLX4):c.2844G>A (p.Ala948=)
Allele change: Synonymous_A948A

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group P

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.