Variant (rsID / SNP)

rs339285

rs339285 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTN4. Location: chromosome 3, position 3,081,825. The table records no clinical significance for this variant.

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Reference-table entries

CNTN4Not classified

Variant type: synonymous_variant
Chromosome / position: 3:3081825
HGVS: NM_001206955.2,c.2268T>C,p.Asp756Asp
Allele change: Synonymous_D756D

Associated conditions / phenotypes

Silent

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.