Variant (rsID / SNP)
rs114088633
rs114088633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORBS1. Location: chromosome 10, position 97,096,555. The table records no clinical significance for this variant.
Reference-table entries
SORBS1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:97096555
- HGVS
- NM_001384452.1,c.4238G>A,p.Arg1413His
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Missense_R1121H|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.