Variant (rsID / SNP)
rs3764147
rs3764147 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LACC1. Location: chromosome 13, position 44,457,925. The table records no clinical significance for this variant.
Reference-table entries
LACC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 13:44457925
- HGVS
- NM_001128303.2,c.760A>G,p.Ile254Val
- Allele change
- Silent
Associated conditions / phenotypes
Leprosy 3|Lepromatous Leprosy|Erythema Nodosum|Inflammatory Bowel Disease|Colitis|Ulcerative Colitis|Disease by Infectious Agent|Inflammatory Spondylopathy|Spondyloarthropathy 1|Ileitis|Spondylitis|Crohn's Disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.