Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28934906
rs28934906
0.716 0.320 X 154031355 missense variant G/A snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 1.000 6 2000 2010
dbSNP: rs1553630279
rs1553630279
0.807 0.160 3 41225049 stop gained C/T snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 1.000 3 1989 2017
dbSNP: rs1476413
rs1476413
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.020 1.000 2 2011 2016
dbSNP: rs1800795
rs1800795
0.494 0.840 7 22727026 intron variant C/G snv 0.71
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.020 1.000 2 2011 2013
dbSNP: rs1001179
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs1005573
rs1005573
0.925 0.080 21 33026408 5 prime UTR variant C/T snv 0.73
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2019 2019
dbSNP: rs1042714
rs1042714
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2005 2005
dbSNP: rs10431386
rs10431386
1.000 0.040 12 120691123 intron variant C/T snv 0.34
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2018 2018
dbSNP: rs1057519583
rs1057519583
0.882 0.160 10 103900115 missense variant C/G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2019 2019
dbSNP: rs10774909
rs10774909
1.000 0.040 12 117236324 intron variant C/G snv 0.28
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2018 2018
dbSNP: rs1126616
rs1126616
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs11728697
rs11728697
0.925 0.080 4 87977789 non coding transcript exon variant C/T snv 0.54 0.46
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs1191926239
rs1191926239
0.807 0.200 9 117704539 missense variant C/G snv 4.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2009 2009
dbSNP: rs1217401
rs1217401
0.925 0.080 1 113896329 missense variant A/G snv 0.30 0.42
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2013 2013
dbSNP: rs1217691063
rs1217691063
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2005 2005
dbSNP: rs121918399
rs121918399
0.925 0.120 19 44907843 missense variant C/T snv 8.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs1411040
rs1411040
1.000 0.040 13 110291574 intron variant C/T snv 0.84
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs1477816966
rs1477816966
1.000 0.040 7 151010703 missense variant A/G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2005 2005
dbSNP: rs16944
rs16944
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2019 2019
dbSNP: rs1799724
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2016 2016
dbSNP: rs1800796
rs1800796
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs1800871
rs1800871
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2018 2018
dbSNP: rs1801131
rs1801131
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2011 2011
dbSNP: rs190853081
rs190853081
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2014 2014
dbSNP: rs191727850
rs191727850
1.000 0.040 8 64379319 intron variant A/G snv 1.0E-04
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.010 1.000 1 2018 2018