Variant (rsID / SNP)
rs2302188
rs2302188 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CEACAM21. Location: chromosome 19, position 42,085,873. The table records no clinical significance for this variant.
Reference-table entries
CEACAM21Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:42085873
- HGVS
- NM_001098506.4,c.592A>G,p.Met198Val
- Allele change
- Missense_M70V
Associated conditions / phenotypes
Type 1 Diabetes Mellitus 19
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.