Variant (rsID / SNP)

rs11132305

rs11132305 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC110. Location: chromosome 4, position 186,377,534. The table records no clinical significance for this variant.

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Reference-table entries

CCDC110Not classified

Variant type: intron_variant
Chromosome / position: 4:186377534
HGVS: NM_152775.4,c.2461+1746G>A
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.