Variant (rsID / SNP)
rs443198
rs443198 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOTCH4. Location: chromosome 6, position 32,190,406. The table records no clinical significance for this variant.
Reference-table entries
NOTCH4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32190406
- HGVS
- NM_004557.4,c.333T>C,p.Gly111Gly
- Allele change
- Silent
Associated conditions / phenotypes
Mycobacterium Tuberculosis 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
