Variant (rsID / SNP)

rs35008315

rs35008315 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDHR3. Location: chromosome 7, position 105,615,406. The table records no clinical significance for this variant.

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Reference-table entries

CDHR3Not classified

Variant type: missense_variant
Chromosome / position: 7:105615406
HGVS: NM_152750.5,c.163G>A,p.Val55Met
Allele change: Missense_V55M

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.