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Variant (rsID / SNP)

rs1026158

CCDC168

rs1026158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC168. Location: chromosome 13, position 103,400,083. The table records no clinical significance for this variant.

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Reference-table entries

CCDC168Not classified
Variant type
synonymous_variant
Chromosome / position
13:103400083
HGVS
NM_001146197.3,c.2964C>T,p.Ser988Ser
Allele change
Synonymous_S988S

Public references

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