Variant (rsID / SNP)
rs1558878
rs1558878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARSG. Location: chromosome 17, position 66,364,804. The table records no clinical significance for this variant.
Reference-table entries
ARSGNot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:66364804
- HGVS
- NM_001267727.2,c.820T>C,p.Trp274Arg
- Allele change
- Missense_W273R
Associated conditions / phenotypes
Missense_W274R|Missense_W258R|Missense_W274R|Missense_W273R|Missense_W274R|Missense_W274R|Missense_W274R|Missense_W274R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.