Table 1. Frequencies of the different haplotypes in HSCR cases with and without the RETR114H mutation.
RET starts | ||||||||||||||||||||||||||||||
rs2795500 | rs2744088 | rs2744085 | rs12768318 | rs3121323 | rs2488291 | rs11239832 | rs788273 | rs788261 | rs7908085 | rs2185792 | rs10900290 | rs947699 | rs2082106 | rs3026720* | rs741763* | rs2505995 | rs10900296* | rs10900297* | rs2506011 | rs1864410* | rs2435364* | rs2435362* | rs2435357* | rs2435356 | rs2506021 | rs2435342 | rs752975* | rs2505538 | rs2505535* | rs2505533 |
21 SNPs plus R114H sequencing data haplotype estimates: | ||||||||||||||||||||||||||||||
T | G | A | C | A | A | A | T | A | G | |||||||||||||||||||||
67 SNPs plus R114H genome-wide and sequencing data haplotype estimates: | ||||||||||||||||||||||||||||||
T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A | ||||||||||||||
T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A | ||||||||||||||
T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A | ||||||||||||||
T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A | ||||||||||||||
A | G | C | A | G | A | G | T | G | A | G | C | A | C | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | C | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | C | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | G | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | G | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | G | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | G | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
A | G | C | A | G | A | G | T | G | A | G | C | A | G | T | G | T | A | C | A | A | A | A | T | A | G | T | A | T | G | A |
*genotyped as part of original sample.
M = mutant allele (A).