RS148234606 SLC52A2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Brown-Vialetto-van Laere syndrome 2
Inborn genetic diseases
SLC52A2-related disorder
Brown-Vialetto-van Laere syndrome 2
Inborn genetic diseases
SLC52A2-related disorder
Other Variants in SLC52A2