Variant (rsID / SNP)
rs915894
rs915894 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOTCH4. Location: chromosome 6, position 32,190,390. The table records no clinical significance for this variant.
Reference-table entries
NOTCH4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:32190390
- HGVS
- NM_004557.4,c.349A>C,p.Lys117Gln
- Allele change
- Silent
Associated conditions / phenotypes
Lung Disease|Schizophrenia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
