Variant (rsID / SNP)

rs2028414

rs2028414 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP170B. Location: chromosome 14, position 105,349,388. The table records no clinical significance for this variant.

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Reference-table entries

CEP170BNot classified

Variant type: synonymous_variant
Chromosome / position: 14:105349388
HGVS: NM_001112726.3,c.594A>C,p.Pro198Pro
Allele change: Synonymous_P128P

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.