Variant (rsID / SNP)
rs55788818
rs55788818 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIMS2. Location: chromosome 8, position 105,105,846. The table records no clinical significance for this variant.
Reference-table entries
RIMS2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 8:105105846
- HGVS
- NM_001348484.3,c.3841C>T,p.Arg1281Cys
- Allele change
- Silent
Associated conditions / phenotypes
Silent|Missense_R1194C|Silent|Silent|Silent|Missense_R949C|Silent|Missense_R998C|Silent|Missense_R998C|Silent|Silent|Missense_R1030C|Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.