Variant (rsID / SNP)

rs190743758

rs190743758 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SOST. Location: chromosome 17, position 41,836,119. Clinical significance in the table: Likely benign.

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Reference-table entries

SOSTLikely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 17:41836119
Cytoband: 17q21.31
HGVS: NM_025237.3(SOST):c.-10G>A
Allele change: Silent

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.