Variant (rsID / SNP)

rs4918979

rs4918979 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CC2D2B. Location: chromosome 10, position 97,698,370. The table records no clinical significance for this variant.

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Reference-table entries

CC2D2BNot classified

Variant type: synonymous_variant
Chromosome / position: 10:97698370
HGVS: NM_001349008.3,c.580C>T,p.Leu194Leu
Allele change: Silent

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.