Variant (rsID / SNP)

rs1181883

rs1181883 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC27. Location: chromosome 1, position 3,677,933. The table records no clinical significance for this variant.

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Reference-table entries

CCDC27Not classified

Variant type: missense_variant
Chromosome / position: 1:3677933
HGVS: NM_152492.3,c.800T>C,p.Met267Thr
Allele change: Missense_M267T

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.