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Table 2 Candidate genes in SAH identified by burden test of rare variants

From: Exome sequencing study revealed novel susceptibility loci in subarachnoid hemorrhage (SAH)

GeneNumber of Cases with mutationsNumber of Controls with mutationsNumber of Cases without mutationsNumber of Controls without mutationsP valueOR
OBSCN261168820.0052.834
ABCG87087930.007Inf
PIGG7087930.007Inf
GOLGA26088930.015Inf
MTMR46088930.015Inf
MYH16088930.015Inf
OTOGL6088930.015Inf
TCF36088930.015Inf
TJP110284910.0175.374
KMT2C8186920.0188.482
ADGRV116678870.0212.958
FBN39285910.0304.782
ABCG55089930.030Inf
BCL95089930.030Inf
C1orf945089930.030Inf
CEBPZ5089930.030Inf
COG35089930.030Inf
CTC15089930.030Inf
FDXR5089930.030Inf
GRIK35089930.030Inf
INCENP5089930.030Inf
IQGAP35089930.030Inf
KNDC15089930.030Inf
LETMD15089930.030Inf
METTL225089930.030Inf
NCOA65089930.030Inf
PDZD75089930.030Inf
PIF15089930.030Inf
PLXNA45089930.030Inf
RAPGEFL15089930.030Inf
RGS145089930.030Inf
SCN7A5089930.030Inf
THEG5089930.030Inf
VEPH15089930.030Inf
ZFP905089930.030Inf
LENG87187920.0337.339
NIPBL7187920.0337.339
TECPR27187920.0337.339