Variant (rsID / SNP)
rs723077
rs723077 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTC12. Location: chromosome 11, position 113,194,168. The table records no clinical significance for this variant.
Reference-table entries
TTC12Not classified
- Variant type
- missense_variant
- Chromosome / position
- 11:113194168
- HGVS
- NM_001318533.2,c.217A>C,p.Met73Leu
- Allele change
- Missense_M73L
Associated conditions / phenotypes
Alcohol Dependence
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.