Variant (rsID / SNP)
rs2229498
rs2229498 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SRGN. Location: chromosome 10, position 70,856,852. The table records no clinical significance for this variant.
Reference-table entries
SRGNNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:70856852
- HGVS
- NM_001321053.2,c.92G>A,p.Arg31Gln
- Allele change
- Missense_R31Q
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.