Variant (rsID / SNP)

rs77591659

rs77591659 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP135. Location: chromosome 4, position 56,820,412. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CEP135Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 4:56820412
Cytoband: 4q12
HGVS: NM_025009.5(CEP135):c.335G>A (p.Arg112His)
Allele change: Missense_R112H

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.