Variant (rsID / SNP)

rs115491049

rs115491049 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLX4. Location: chromosome 16, position 3,639,571. Clinical significance in the table: Benign.

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Reference-table entries

SLX4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 16:3639571
Cytoband: 16p13.3
HGVS: NM_032444.4(SLX4):c.4068G>A (p.Pro1356=)
Allele change: Synonymous_P1356P

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.