Source: CLINVAR

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: rs869320624
rs869320624
0.776 0.400 1 19220814 frameshift variant AAGG/- delins 1.4E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 2 2016 2017
dbSNP: rs121908188
rs121908188
0.742 0.360 1 25809753 missense variant G/A;C snv 1.8E-04
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs199564797
rs199564797
0.742 0.360 1 25809150 missense variant G/A snv 1.2E-05 1.4E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs745886248
rs745886248
0.742 0.360 1 25811710 missense variant G/A;C;T snv 4.3E-06; 4.3E-06; 4.3E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs765379963
rs765379963
0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1553403917
rs1553403917
0.807 0.320 2 73451171 frameshift variant -/A delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2018 2018
dbSNP: rs797045164
rs797045164
0.851 0.120 2 240785063 missense variant G/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2016 2016
dbSNP: rs267607261
rs267607261
0.807 0.280 2 27312753 stop gained C/T snv 8.0E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs368900406
rs368900406
0.827 0.160 2 27312255 non coding transcript exon variant A/C snv 8.0E-06 2.1E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs587776917
rs587776917
0.776 0.200 2 232485937 stop gained -/T delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs886041287
rs886041287
0.882 0.160 2 178535594 frameshift variant -/GT delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs431905504
rs431905504
0.776 0.280 5 1411242 splice donor variant C/T snv 6.4E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2012 2012
dbSNP: rs587784105
rs587784105
0.732 0.440 5 177235863 stop gained G/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs587784177
rs587784177
0.790 0.280 5 177283827 missense variant G/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1561881909
rs1561881909
0.925 0.200 6 43044835 frameshift variant G/- delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2019 2019
dbSNP: rs1561892336
rs1561892336
0.807 0.200 6 43050050 stop gained C/T snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2019 2019
dbSNP: rs1561898352
rs1561898352
0.882 0.200 6 43052582 frameshift variant -/A delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2019 2019
dbSNP: rs1010184002
rs1010184002
0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1554208945
rs1554208945
0.752 0.240 6 87260207 missense variant A/C snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs61753219
rs61753219
0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs772887102
rs772887102
0.807 0.200 6 87548623 missense variant A/C snv 2.2E-04 2.8E-05
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs781417096
rs781417096
0.807 0.200 6 87514995 frameshift variant T/- delins 1.6E-05 7.0E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1057520063
rs1057520063
0.763 0.200 7 41964641 frameshift variant -/A delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1178187217
rs1178187217
0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1554317002
rs1554317002
0.724 0.440 7 39950821 frameshift variant C/- delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0