Variant (rsID / SNP)

rs12665607

rs12665607 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,946,629. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CCDC170Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:151946629
Cytoband: 6q25.1
HGVS: NC_000006.12:g.151625494T>A

Associated conditions / phenotypes

Estrogen resistance syndrome

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.