Variant (rsID / SNP)

rs2273510

rs2273510 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CCDC28A. Location: chromosome 6, position 139,097,232. The table records no clinical significance for this variant.

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Reference-table entries

CCDC28ANot classified

Variant type: 5_prime_UTR_premature_start_codon_gain_variant
Chromosome / position: 6:139097232
HGVS: NM_015439.3,c.-26C>T
Allele change: Missense_P82L

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.