Variant (rsID / SNP)

rs62000999

rs62000999 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP72. Location: chromosome 5, position 637,637. The table records no clinical significance for this variant.

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Reference-table entries

CEP72Not classified

Variant type: missense_variant
Chromosome / position: 5:637637
HGVS: NM_018140.4,c.910A>G,p.Met304Val
Allele change: Missense_M304V

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.