Variant (rsID / SNP)

rs8039150

rs8039150 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPRED1. Location: chromosome 15, position 38,647,695. Clinical significance in the table: Benign.

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Reference-table entries

SPRED1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:38647695
Cytoband: 15q14
HGVS: NM_152594.3(SPRED1):c.*3830G>A
Allele change: Silent

Associated conditions / phenotypes

Legius syndrome

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.