Variant (rsID / SNP)

rs928814

rs928814 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPANK1, CSNK2B. Location: chromosome 6, position 31,631,907. The table records no clinical significance for this variant.

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Reference-table entries

GPANK1Not classified

Variant type: synonymous_variant
Chromosome / position: 6:31631907
HGVS: NM_001199237.1,c.349C>T,p.Leu117Leu
Allele change: Synonymous_L117L

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.