Variant (rsID / SNP)

rs7629936

rs7629936 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDHR4. Location: chromosome 3, position 49,836,707. The table records no clinical significance for this variant.

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Reference-table entries

CDHR4Not classified

Variant type: synonymous_variant
Chromosome / position: 3:49836707
HGVS: NM_001007540.4,c.213C>T,p.Ala71Ala
Allele change: Synonymous_A71A

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.