Variant (rsID / SNP)

rs35822882

rs35822882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLIC5. Location: chromosome 6, position 45,916,999. Clinical significance in the table: Benign.

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Reference-table entries

CLIC5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:45916999
Cytoband: 6p21.1
HGVS: NM_016929.5(CLIC5):c.293C>A (p.Pro98His)
Allele change: Missense_P257H

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.