Variant (rsID / SNP)
rs10893053
rs10893053 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GRAMD1B. Location: chromosome 11, position 123,480,981. The table records no clinical significance for this variant.
Reference-table entries
GRAMD1BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:123480981
- HGVS
- NM_001387024.1,c.1854T>C,p.His618His
- Allele change
- Synonymous_H435H
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.