Variant (rsID / SNP)

rs1064319

rs1064319 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC60. Location: chromosome 12, position 119,866,533. The table records no clinical significance for this variant.

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Reference-table entries

CCDC60Not classified

Variant type: missense_variant
Chromosome / position: 12:119866533
HGVS: NM_178499.5,c.136A>G,p.Ile46Val
Allele change: Missense_I46V

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.