Variant (rsID / SNP)
rs415929
rs415929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOTCH4. Location: chromosome 6, position 32,189,032. The table records no clinical significance for this variant.
Reference-table entries
NOTCH4Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:32189032
- HGVS
- NM_004557.4,c.522A>G,p.Thr174Thr
- Allele change
- Silent
Associated conditions / phenotypes
Schizophrenia|Mycobacterium Tuberculosis 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.