Variant (rsID / SNP)
rs7091756
rs7091756 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IDI1. Location: chromosome 10, position 1,094,906. The table records no clinical significance for this variant.
Reference-table entries
IDI1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:1094906
- HGVS
- NM_004508.4,c.38G>A,p.Cys13Tyr
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.