Variant (rsID / SNP)

rs2073711

rs2073711 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CILP. Location: chromosome 15, position 65,494,212. Clinical significance in the table: risk factor.

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Reference-table entries

CILPRisk factor

Clinical significance (as recorded): risk factor
Variant type: single nucleotide variant
Chromosome / position: 15:65494212
Cytoband: 15q22.31
HGVS: NM_003613.4(CILP):c.1184T>C (p.Ile395Thr)
Allele change: Missense_I395T

Associated conditions / phenotypes

Lumbar disc disease, susceptibility to

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.