Variant (rsID / SNP)

rs373577135

rs373577135 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCNKA. Location: chromosome 1, position 16,349,188. Clinical significance in the table: Uncertain significance.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CLCNKAUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:16349188
Cytoband: 1p36.13
HGVS: NM_004070.4(CLCNKA):c.74G>A (p.Cys25Tyr)
Allele change: Missense_C25Y

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.