Variant (rsID / SNP)

rs9546785

rs9546785 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC169. Location: chromosome 13, position 36,801,415. The table records no clinical significance for this variant.

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Reference-table entries

CCDC169Not classified

Variant type: missense_variant
Chromosome / position: 13:36801415
HGVS: NM_001198908.2,c.649G>A,p.Gly217Arg
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.