Variant (rsID / SNP)

rs10838518

rs10838518 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC35C1. Location: chromosome 11, position 45,834,466. Clinical significance in the table: Benign.

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Reference-table entries

SLC35C1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:45834466
Cytoband: 11p11.2
HGVS: NM_018389.5(SLC35C1):c.*1580C>T
Allele change: Silent

Associated conditions / phenotypes

Leukocyte adhesion deficiency type II

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.