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Variant (rsID / SNP)

rs2287791

CCDC106

rs2287791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC106. Location: chromosome 19, position 56,162,776. The table records no clinical significance for this variant.

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Reference-table entries

CCDC106Not classified
Variant type
synonymous_variant
Chromosome / position
19:56162776
HGVS
NM_001370467.1,c.441C>T,p.Ser147Ser
Allele change
Synonymous_S147S

Public references

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