Variant (rsID / SNP)
rs7125943
rs7125943 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IGSF22. Location: chromosome 11, position 18,735,947. The table records no clinical significance for this variant.
Reference-table entries
IGSF22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:18735947
- HGVS
- NM_173588.4,c.1675A>G,p.Met559Val
- Allele change
- Missense_M559V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.