Table 3.
Reason |
Change | SNVs and Affected Alleles |
---|---|---|
Standardization | Intronic SNVs were removed | *26, *27, *29 |
Comments removed | *1B−D, *2A−C, *3A+B, *11A+B, *15, *24, *26, *27, *29 | |
Revised alleles after removing SNVs that are outside of the region used to define haplotypes | *2B, *11B, *27 | |
Merged alleles after removing SNVs that are outside the region used to define haplotypes |
*1.002 and *1.003; *2.001 and *2.002 |
|
Retired after its only defining SNV was removed due to being outside the region used to define haplotype |
*1D
|
|
Revised | *3A, *3B, *8 | |
Other | Correction | *26 (c.-1565C>T was erroneously listed as 1565C>T) |