Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1060499558
rs1060499558
GLI3
2 0.925 0.080 7 41965438 frameshift variant C/- delins 0.700 1.000 1 2017 2017
dbSNP: rs1057520063
rs1057520063
GLI3
13 0.763 0.200 7 41964641 frameshift variant -/A delins 0.700 0
dbSNP: rs144078282
rs144078282
CLPB
9 0.776 0.400 11 72302339 missense variant T/A;C snv 1.8E-04; 2.0E-04 0.700 0
dbSNP: rs1554317931
rs1554317931
GLI3
11 0.851 0.080 7 42045460 frameshift variant G/- delins 0.700 0
dbSNP: rs1555202697
rs1555202697
BBS10
5 0.882 0.160 12 76347446 missense variant C/T snv 0.700 0
dbSNP: rs1559307932
rs1559307932
PDE6D
8 0.807 0.360 2 231737190 frameshift variant -/C ins 0.700 0
dbSNP: rs199476133
rs199476133
ATP6 ; ATP8 ; COX3 ; ND3 ; ND4 ; ND4L
18 0.742 0.320 MT 8993 missense variant T/C;G snv 0.700 0
dbSNP: rs200203460
rs200203460
CLPB
9 0.776 0.400 11 72302312 stop gained G/A;C;T snv 2.8E-05 0.700 0
dbSNP: rs398123425
rs398123425
ATRX
9 0.776 0.320 X 77688876 missense variant T/C snv 0.700 0
dbSNP: rs758361736
rs758361736
KIF7
16 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 0.700 0
dbSNP: rs768933093
rs768933093
BBS10
10 0.807 0.240 12 76348214 missense variant G/A snv 4.8E-05 4.9E-05 0.700 0