This SNP is reported by one or more services.
|| T/G/A (transliterated to +)
||Minor Allele Frequency
||Orientation (dbSNP)|| - (negative/reverse strand)
| Intergenic, near UGT1A1*28.|
| CHR2-LOC100286922 is the genomic location for the rs4124874 near UGT1A1*28 which is associated with Gilbert syndrome due to possible incomplete linkage disequilibrium. |