Variant (rsID / SNP)
rs1126671
rs1126671 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADH4. Location: chromosome 4, position 100,048,414. The table records no clinical significance for this variant.
Reference-table entries
ADH4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 4:100048414
- HGVS
- NM_001306171.2,c.982A>G,p.Ile328Val
- Allele change
- Silent
Associated conditions / phenotypes
Cluster Headache|Headache|Alcohol Use Disorder|Alcohol Dependence|Fabry Disease|Toxic Encephalopathy|Cocaine Dependence|Opioid Addiction|Drug Dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.