Variant (rsID / SNP)

rs3749191

rs3749191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDCP1. Location: chromosome 3, position 45,134,822. The table records no clinical significance for this variant.

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Reference-table entries

CDCP1Not classified

Variant type: missense_variant
Chromosome / position: 3:45134822
HGVS: NM_022842.5,c.1574A>G,p.Gln525Arg
Allele change: Missense_Q525R

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.