Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs141687678

SLX4

rs141687678 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLX4. Location: chromosome 16, position 3,646,371. Clinical significance in the table: Conflicting interpretations of pathogenicity.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SLX4Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
16:3646371
Cytoband
16p13.3
HGVS
NM_032444.4(SLX4):c.1707G>A (p.Pro569=)
Allele change
Synonymous_P569P

Associated conditions / phenotypes

Fanconi anemia|Fanconi anemia complementation group P

Public references

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