Variant (rsID / SNP)

rs2289433

rs2289433 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CORIN. Location: chromosome 4, position 47,839,929. The table records no clinical significance for this variant.

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Reference-table entries

CORINNot classified

Variant type: missense_variant
Chromosome / position: 4:47839929
HGVS: NM_006587.4,c.38G>A,p.Cys13Tyr
Allele change: Missense_C13Y

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.