Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
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
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6517135
rs6517135
0.925 0.080 21 33025263 intron variant T/C snv 0.33
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs6517137
rs6517137
0.882 0.120 21 33028471 3 prime UTR variant T/C snv 0.11
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs9653711
rs9653711
0.851 0.120 21 33029641 intron variant G/A;C snv
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
Nervous System Diseases 0.010 1.000 1 2019 2019