Variant (rsID / SNP)
rs90951
rs90951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLEC10A. Location: chromosome 17, position 6,981,397. The table records no clinical significance for this variant.
Reference-table entries
CLEC10ANot classified
- Variant type
- missense_variant
- Chromosome / position
- 17:6981397
- HGVS
- NM_182906.4,c.103T>C,p.Cys35Arg
- Allele change
- Missense_C35R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.