Variant (rsID / SNP)
rs422951
rs422951 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NOTCH4. Location: chromosome 6, position 32,188,383. The table records no clinical significance for this variant.
Reference-table entries
NOTCH4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:32188383
- HGVS
- NM_004557.4,c.958A>G,p.Thr320Ala
- Allele change
- Silent
Associated conditions / phenotypes
Hepatitis B|Multiple Sclerosis|Hepatocellular Carcinoma|Hepatitis|Demyelinating Disease|Neuromyelitis Optica|Mycobacterium Tuberculosis 1|Schizophrenia|Alcoholic Liver Cirrhosis|Inclusion Body Myositis|Myositis|Liver Cirrhosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.