Variant (rsID / SNP)

rs1800169

rs1800169 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CNTF. Location: chromosome 11, position 58,391,501. Clinical significance in the table: Benign.

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Reference-table entries

CNTFBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:58391501
Cytoband: 11q12.1
HGVS: NM_000614.4(CNTF):c.115-6G>A
Allele change: Silent

Associated conditions / phenotypes

CILIARY NEUROTROPHIC FACTOR POLYMORPHISM

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.