Variant (rsID / SNP)

rs199777941

rs199777941 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP152. Location: chromosome 15, position 49,036,492. Clinical significance in the table: Likely benign.

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Reference-table entries

CEP152Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 15:49036492
Cytoband: 15q21.1
HGVS: NM_001194998.2(CEP152):c.3780G>T (p.Gly1260=)
Allele change: Synonymous_G1204G

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.