Variant (rsID / SNP)

rs14365

rs14365 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSNK2B. Location: chromosome 6, position 31,635,710. The table records no clinical significance for this variant.

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Reference-table entries

CSNK2BNot classified

Variant type: synonymous_variant
Chromosome / position: 6:31635710
HGVS: NM_001320.7,c.138T>C,p.Tyr46Tyr
Allele change: Synonymous_Y46Y

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.