Variant (rsID / SNP)
rs628031
rs628031 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A1. Location: chromosome 6, position 160,560,845. The table records no clinical significance for this variant.
Reference-table entries
SLC22A1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 6:160560845
- HGVS
- NM_003057.3,c.1222A>G,p.Met408Val
- Allele change
- Missense_M408V
Associated conditions / phenotypes
Leukemia, Chronic Myeloid|Myeloid Leukemia|Type 2 Diabetes Mellitus|Diabetes Mellitus|Pure Autonomic Failure|Epilepsy|Polycystic Ovary Syndrome|Hypoglycemia|Telangiectasis|Ataxia and Polyneuropathy, Adult-Onset|Ataxia-Telangiectasia|Leukemia|Rem Sleep Behavior Disorder|Lipid Metabolism Disorder|Tremor
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.