Variant (rsID / SNP)
rs4371716
rs4371716 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDH12. Location: chromosome 5, position 22,078,584. The table records no clinical significance for this variant.
Reference-table entries
CDH12Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:22078584
- HGVS
- NM_001317227.2,c.202G>A,p.Val68Met
- Allele change
- Missense_V68M
Associated conditions / phenotypes
Missense_V68M|Missense_V68M|Missense_V68M
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.