Variant (rsID / SNP)

rs803064

rs803064 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CUX1. Location: chromosome 7, position 101,917,521. The table records no clinical significance for this variant.

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Reference-table entries

CUX1Not classified

Variant type: missense_variant
Chromosome / position: 7:101917521
HGVS: NM_001202544.3,c.1342G>A,p.Ala448Thr
Allele change: Missense_A448T

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.