Variant (rsID / SNP)
rs1126667
rs1126667 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALOX12. Location: chromosome 17, position 6,902,760. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 17:6902760
- HGVS
- NM_000697.3,c.782A>G,p.Gln261Arg
- Allele change
- Silent
Associated conditions / phenotypes
Schizophrenia|Breast Cancer|Psoriasis 12|Pustulosis of Palm and Sole|Psoriasis|Sickle Cell Disease|Osteoporosis|Body Mass Index Quantitative Trait Locus 11|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Bone Mineral Density Quantitative Trait Locus 15|Body Mass Index Quantitative Trait Locus 14|Bone Mineral Density Quantitative Trait Locus 8|Body Mass Index Quantitative Trait Locus 9
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.