Variant (rsID / SNP)
rs657723
rs657723 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARL5C. Location: chromosome 17, position 37,319,103. The table records no clinical significance for this variant.
Reference-table entries
ARL5CNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:37319103
- HGVS
- NM_001143968.1,c.116A>G,p.Asn39Ser
- Allele change
- Missense_N39S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.