SNP ID | SNP effect | Number of patients with variant (nā=ā100) | Ethnicitya |
---|---|---|---|
c.71Cā>āG | 5ā UTR | 3 | W |
345Gā>āA | Synonymous | 1 | W |
531ā+ā10Gā>āC | Intronic | 9 | W |
933Cā>āG | Synonymous | 1 | AA |
1680Gā>āC | Synonymous | 1 | W |
A592T | Missense | 1 | HS |
A617T | Missense | 1 | AA |
1896Cā>āT | Synonymous | 2 | AA |
2076Ā Tā>āC | Synonymous | 46 | W, AA, HS, NA |
1937-13Ā Tā>āC | Intronic | 6 | W |
95971Cā>āT | Synonymous | 6 | W |
P825L | Missense | 1 | W |
G879S | Missense | 1 | W |
101193Cā>āA | Synonymous | 2 | AA |