Variant (rsID / SNP)

rs6929137

rs6929137 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC170. Location: chromosome 6, position 151,936,677. Clinical significance in the table: Benign.

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Reference-table entries

CCDC170Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:151936677
Cytoband: 6q25.1
HGVS: NM_025059.4(CCDC170):c.1810G>A (p.Val604Ile)
Allele change: Missense_V604I

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.