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: rs1060499939
rs1060499939
0.882 0.120 2 32137172 missense variant G/C;T snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1131692230
rs1131692230
0.807 0.160 X 19353124 missense variant A/G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs121918455
rs121918455
0.695 0.440 12 112477720 missense variant A/C;G snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1345176461
rs1345176461
0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1554208945
rs1554208945
0.752 0.240 6 87260207 missense variant A/C snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1555247672
rs1555247672
0.827 0.200 12 116007542 stop gained G/A snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1555303073
rs1555303073
0.851 0.120 13 110176912 missense variant C/T snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs1555377415
rs1555377415
0.827 0.200 14 77027274 stop gained G/C snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs28936415
rs28936415
0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs564185858
rs564185858
0.882 0.040 10 110122249 missense variant G/A snv 1.2E-05 1.4E-05
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs606231435
rs606231435
0.827 0.240 19 41970539 missense variant C/T snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs61749721
rs61749721
0.732 0.200 X 154031065 stop gained G/A snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs756421370
rs756421370
0.807 0.120 1 29200513 splice donor variant -/A delins 1.4E-04 6.3E-05
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs767399782
rs767399782
0.925 0.120 19 6495736 missense variant C/A;T snv 4.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs780533096
rs780533096
0.701 0.600 13 23886338 missense variant C/G;T snv 4.8E-06; 9.6E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs80338700
rs80338700
0.851 0.200 16 8806398 missense variant C/G;T snv 4.0E-06; 2.4E-05
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
dbSNP: rs937726878
rs937726878
0.882 0.240 16 8797949 splice donor variant G/T snv 1.4E-05 7.0E-06
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0.700 0
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