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Variant (rsID / SNP)

rs6494466

CSNK1G1

rs6494466 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CSNK1G1. Location: chromosome 15, position 64,508,763. The table records no clinical significance for this variant.

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Reference-table entries

CSNK1G1Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
15:64508763
HGVS
NM_001329605.2,c.442C>T,p.Leu148Leu
Allele change
Synonymous_L148L

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.