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. 2022 May 11;109(6):1105–1116. doi: 10.1016/j.ajhg.2022.04.011

Table 1.

Clinical and molecular summary of the three case-control datasets

UCSF-Mayo
cases N = 1,973
GICC
controls N = 1,859
AGS i370 cases
N = 659
AGS i370 controls N = 586 TCGA
cases N = 786
WTCCC
controls N = 5,711
Age

<40 983 (50%) 538 (29%) 101 (15%) 85 (15%) 213 (27%) 0 (0%)
40–59 476 (24%) 555 (30%) 329 (50%) 252 (43%) 279 (36%) 0 (0%)
≥60 514 (26%) 766 (41%) 229 (35%) 249 (42%) 245 (31%) 0 (0%)
Missing 0 (0%) 0 (0%) 0 (0%) 0 (0%) 49 (6%) 5,711 (100%)

Sex

Female 822 (42%) 744 (40%) 229 (35%) 280 (48%) 328 (42%) 2,819 (49%)
Male 1,151 (58%) 1,115 (60%) 430 (65%) 306 (52%) 458 (58%) 2,892 (51%)

IDH mutation status

Mutant 588 (30%) N/A 111 (17%) N/A 375 (48%) N/A
Wild type 699 (35%) N/A 416 (63%) N/A 364 (46%) N/A
Missing 686 (35%) N/A 132 (20%) N/A 47 (6%) N/A

Molecular subtype based on IDH mutation and 1p/19q codeletion

MT-codel 244 (12%) N/A 9 (1%) N/A 143 (18%) N/A
MT-noncodel 291 (15%) N/A 94 (14%) N/A 230 (29%) N/A
WT-noncodel 507 (26%) N/A 416 (63%) N/A 357 (46%) N/A
Missing/other 905 (47%) N/A 140 (22%) N/A 56 (7%) N/A

N/A, not applicable to controls.