Variant (rsID / SNP)

rs9849237

rs9849237 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTN4. Location: chromosome 3, position 2,675,189. Clinical significance in the table: association.

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Reference-table entries

CNTN4Association

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 3:2675189
Cytoband: 3p26.3
HGVS: NM_175607.3(CNTN4):c.55+61947C>T
Allele change: Silent

Associated conditions / phenotypes

Lip and oral cavity carcinoma

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.