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Table 6 The potential disease causing SNPs in dominant inheritance pattern for pedigree 2

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

ChrPosFunctionGeneSIFTPp2LRTMTM-CAPCADDREVEL
11.5E+ 08exonicHIST2H2AC0.000.10ND0.0248.00.15
11.52E+ 08exonicRPTN0.010.02.N0.00316.30.01
11.57E+ 08exonicIQGAP30.001.00DD0.15435.00.84
11.62E+ 08exonicDUSP120.101.00DD0.00923.40.16
656,471,328intronicDST0.010.17N.0.03312.00.10
720,782,555exonicABCB50.000.99DD0.03927.80.70
729,132,261exonicCPVL0.040.99ND0.14226.60.47
794,057,039exonicCOL1A20.100.98DN0.08226.20.44
71.01E+ 08exonicMUC170.020.61.N0.0035.60.04
71.51E+ 08exonicCHPF20.030.89DD0.04923.30.32
890,936,937exonicOSGIN20.380.03DD0.0111.30.07
173,030,476exonicOR1G10.050.01.N013.60.03
174,619,845exonicARRB20.040.90DD0.03432.00.15
176,683,525exonicFBXO390.140.09DD0.02419.80.17
177,733,695exonicDNAH20.010.89NN0.00423.80.11