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: rs104894229
rs104894229
0.564 0.600 11 534289 missense variant C/A;G;T snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 9 2005 2009
dbSNP: rs267607144
rs267607144
0.716 0.360 12 109800665 missense variant C/T snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 4 2010 2014
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: rs1114167445
rs1114167445
0.851 0.160 19 40504064 stop gained C/T snv 8.0E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2017 2017
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: rs1555682265
rs1555682265
DCC
0.851 0.160 18 52923796 frameshift variant TTTCTGG/- delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2017 2017
dbSNP: rs1557055405
rs1557055405
0.807 0.400 X 153743532 missense variant T/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 1998 1998
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: rs202193096
rs202193096
0.925 0.040 16 30089130 missense variant G/A snv 2.2E-04 1.0E-04
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 1.000 1 2015 2015
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: 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: rs1009298200
rs1009298200
0.742 0.400 16 5079077 missense variant C/G;T snv 7.0E-06
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
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: rs1057518789
rs1057518789
0.925 0.040 16 3728803 stop gained G/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1057518812
rs1057518812
0.827 0.240 15 48430742 missense variant T/A snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1057518828
rs1057518828
1.000 0.040 17 44911317 missense variant T/G snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1057518891
rs1057518891
0.851 0.120 8 60854479 stop gained C/T snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1057518908
rs1057518908
0.882 0.120 12 47984112 missense variant C/T snv
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: rs1060505041
rs1060505041
0.716 0.400 19 13136099 missense variant C/A;T snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1064793575
rs1064793575
0.925 0.040 X 136016706 frameshift variant GT/- delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1085307132
rs1085307132
0.882 0.160 8 143817668 frameshift variant -/TTTT delins
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0
dbSNP: rs1085308004
rs1085308004
0.807 0.240 15 48425420 missense variant A/G snv
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
0.700 0