Variant (rsID / SNP)
rs41315995
rs41315995 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UNC13B. Location: chromosome 9, position 35,398,605. The table records no clinical significance for this variant.
Reference-table entries
UNC13BNot classified
- Variant type
- missense_variant
- Chromosome / position
- 9:35398605
- HGVS
- NM_001371189.2,c.11887G>A,p.Val3963Ile
- Allele change
- Missense_V1214I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.