Variant (rsID / SNP)

rs17882143

rs17882143 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOST. Location: chromosome 17, position 41,836,082. Clinical significance in the table: Benign.

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Reference-table entries

SOSTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:41836082
Cytoband: 17q21.31
HGVS: NM_025237.3(SOST):c.28G>A (p.Val10Ile)
Allele change: Missense_V10I

Associated conditions / phenotypes

Sclerosteosis 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.