Variant (rsID / SNP)

rs118204008

rs118204008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP27B1. Location: chromosome 12, position 58,157,581. Clinical significance in the table: Pathogenic.

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Reference-table entries

CYP27B1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 12:58157581
Cytoband: 12q14.1
HGVS: NM_000785.4(CYP27B1):c.1226C>T (p.Thr409Ile)
Allele change: Missense_T409I

Associated conditions / phenotypes

Vitamin D-dependent rickets, type 1A

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.