Variant (rsID / SNP)

rs745961

rs745961 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEP89. Location: chromosome 19, position 33,370,070. The table records no clinical significance for this variant.

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Reference-table entries

CEP89Not classified

Variant type: stop_lost
Chromosome / position: 19:33370070
HGVS: NM_032816.5,c.2350T>C,p.Ter784Glnext*?
Allele change: Missense_X784Q

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.