Variant (rsID / SNP)

rs2466773

rs2466773 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP131. Location: chromosome 17, position 79,174,221. The table records no clinical significance for this variant.

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Reference-table entries

CEP131Not classified

Variant type: missense_variant
Chromosome / position: 17:79174221
HGVS: NM_001319228.2,c.814A>G,p.Thr272Ala
Allele change: Missense_T272A

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.