Variant (rsID / SNP)

rs61749689

rs61749689 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP24A1. Location: chromosome 20, position 52,790,005. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

CYP24A1Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 20:52790005
Cytoband: 20q13.2
HGVS: NM_000782.5(CYP24A1):c.114G>T (p.Pro38=)
Allele change: Synonymous_P38P

Associated conditions / phenotypes

Hypercalcemia, infantile, 1

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.