Variant (rsID / SNP)
rs726176
rs726176 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORBS1. Location: chromosome 10, position 97,106,165. The table records no clinical significance for this variant.
Reference-table entries
SORBS1Not classified
- Variant type
- splice_region_variant&synonymous_variant
- Chromosome / position
- 10:97106165
- HGVS
- NM_001384452.1,c.3303A>G,p.Leu1101Leu
- Allele change
- Synonymous_L621L
Associated conditions / phenotypes
Synonymous_L524L|Synonymous_L586L|Synonymous_L779L|Synonymous_L459L|Synonymous_L809L|Synonymous_L591L|Synonymous_L515L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.