Variant (rsID / SNP)

rs3734805

rs3734805 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,939,350. 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: 6:151939350
Cytoband: 6q25.1
HGVS: NM_025059.4(CCDC170):c.*68A>C
Allele change: Silent

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.