Variant (rsID / SNP)

rs58624842

rs58624842 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIL1. Location: chromosome 5, position 138,362,687. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SIL1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:138362687
Cytoband: 5q31.2
HGVS: NM_022464.5(SIL1):c.454-6C>T
Allele change: Silent

Associated conditions / phenotypes

Marinesco-SjÃ¶gren syndrome

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.