Variant (rsID / SNP)
rs2653349
rs2653349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HCRTR2. Location: chromosome 6, position 55,142,337. The table records no clinical significance for this variant.
Reference-table entries
HCRTR2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:55142337
- HGVS
- NM_001384272.1,c.922A>G,p.Ile308Val
- Allele change
- Missense_I308V
Associated conditions / phenotypes
Cluster Headache|Headache|Alzheimer Disease|Goiter|Schizotypal Personality Disorder|Mental Depression|Major Depressive Disorder|Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Depression|Sleep Disorder|Mood Disorder|Narcolepsy|Hypersomnia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.