| Gene | CHR2-LOC100286922 |
Chromosome number |
2 |
Chromosome position |
233757013 |
| Alleles |
T/G/A (transliterated to +) |
Minor Allele |
T |
Minor Allele Frequency |
0.4119 |
| Notation |
G>T |
Clinical significance |
|
Orientation (dbSNP) | - (negative/reverse strand)
|
|
SNP Function |
| Intergenic, near UGT1A1*28. |
|
Gene Function |
| CHR2-LOC100286922 is the genomic location for the rs4124874 near UGT1A1*28 which is associated with Gilbert syndrome due to possible incomplete linkage disequilibrium. |
This SNP is reported by one or more services.
