Variant (rsID / SNP)
rs3746500
rs3746500 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZSWIM1. Location: chromosome 20, position 44,511,533. The table records no clinical significance for this variant.
Reference-table entries
ZSWIM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 20:44511533
- HGVS
- NM_080603.5,c.302G>A,p.Arg101Gln
- Allele change
- Missense_R101Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
