Variant (rsID / SNP)
rs2185724
rs2185724 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to JCAD. Location: chromosome 10, position 30,316,208. The table records no clinical significance for this variant.
Reference-table entries
JCADNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:30316208
- HGVS
- NM_001350022.2,c.2869A>G,p.Arg957Gly
- Allele change
- Missense_R957G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.