present in Gene: HTT
present in Chromosome: 4
Position on Chromosome: 3233253
Alleles of this Variant: G/A;T
rs362272 in
HTT gene and
Huntington Disease
PMID 22387017 2012 Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.
rs362272 in
HTT gene and
Sulfate measurement
PMID 27412988 2016 From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.