Variant (rsID / SNP)

rs12511068

rs12511068 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC149. Location: chromosome 4, position 24,896,658. The table records no clinical significance for this variant.

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Reference-table entries

CCDC149Not classified

Variant type: missense_variant
Chromosome / position: 4:24896658
HGVS: NM_173463.6,c.19G>A,p.Val7Ile
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.