Variant (rsID / SNP)
rs6967330
rs6967330 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDHR3. Location: chromosome 7, position 105,658,451. The table records no clinical significance for this variant.
Reference-table entries
CDHR3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 7:105658451
- HGVS
- NM_152750.5,c.1586G>A,p.Cys529Tyr
- Allele change
- Missense_C529Y
Associated conditions / phenotypes
Childhood-Onset Asthma|Asthma|Ige Responsiveness, Atopic|Common Cold|Pulmonary Disease, Chronic Obstructive|Bronchitis|Allergic Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.