Variant (rsID / SNP)
rs55693639
rs55693639 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGEF10L. Location: chromosome 1, position 17,949,562. The table records no clinical significance for this variant.
Reference-table entries
ARHGEF10LNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:17949562
- HGVS
- NM_018125.4,c.1092C>T,p.Phe364Phe
- Allele change
- Synonymous_F364F
Associated conditions / phenotypes
Synonymous_F142F
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.