Variant (rsID / SNP)

rs8112667

rs8112667 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC105. Location: chromosome 19, position 15,133,926. The table records no clinical significance for this variant.

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Reference-table entries

CCDC105Not classified

Variant type: missense_variant
Chromosome / position: 19:15133926
HGVS: NM_173482.3,c.1495C>A,p.Pro499Thr
Allele change: Missense_P499T

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.