Variant (rsID / SNP)
rs3746887
rs3746887 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to B3GALT5. Location: chromosome 21, position 41,032,740. The table records no clinical significance for this variant.
Reference-table entries
B3GALT5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 21:41032740
- HGVS
- NM_033172.3,c.266T>C,p.Met89Thr
- Allele change
- Missense_M85T
Associated conditions / phenotypes
Missense_M89T|Missense_M85T|Missense_M85T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.