Variant (rsID / SNP)

rs10489579

rs10489579 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SWT1. Location: chromosome 1, position 185,143,721. The table records no clinical significance for this variant.

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Reference-table entries

SWT1Not classified

Variant type: missense_variant
Chromosome / position: 1:185143721
HGVS: NM_001105518.2,c.442A>G,p.Ile148Val
Allele change: Missense_I148V

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.