Variant (rsID / SNP)

rs143360018

rs143360018 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLIC5. Location: chromosome 6, position 45,909,349. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CLIC5Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 6:45909349
Cytoband: 6p21.1
HGVS: NM_016929.5(CLIC5):c.341C>A (p.Ala114Glu)
Allele change: Missense_A273E

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.