Variant (rsID / SNP)

rs192282380

rs192282380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDHR1. Location: chromosome 10, position 85,958,854. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CDHR1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:85958854
Cytoband: 10q23.1
HGVS: NM_033100.4(CDHR1):c.415C>G (p.Pro139Ala)
Allele change: Missense_P139A

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.