Variant (rsID / SNP)
rs2433724
rs2433724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VSTM1. Location: chromosome 19, position 54,545,531. The table records no clinical significance for this variant.
Reference-table entries
VSTM1Not classified
- Variant type
- missense_variant&splice_region_variant
- Chromosome / position
- 19:54545531
- HGVS
- NM_198481.4,c.487A>G,p.Ser163Gly
- Allele change
- Missense_S163G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.