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: rs80356529
rs80356529
OPA1
9 0.827 0.240 3 193643996 missense variant G/A;C snv 0.030 1.000 3 2003 2011
dbSNP: rs119103265
rs119103265
MFN2
5 0.827 0.120 1 12002033 missense variant C/T snv 0.020 1.000 2 2006 2011
dbSNP: rs387906930
rs387906930
WFS1
8 0.790 0.360 4 6301846 missense variant C/G;T snv 0.020 1.000 2 2010 2011
dbSNP: rs104893753
rs104893753
OPA1
2 0.925 0.080 3 193643005 stop gained C/T snv 0.010 1.000 1 2003 2003
dbSNP: rs1057517686
rs1057517686
ATAD3A
7 0.827 0.120 1 1529299 missense variant C/T snv 0.700 1.000 1 2016 2016
dbSNP: rs1177373525
rs1177373525
OPA1 ; LOC102724808
2 0.925 0.080 3 193666331 missense variant A/G snv 1.2E-05 0.010 1.000 1 2019 2019
dbSNP: rs1231502335
rs1231502335
OPA1
1 1.000 0.080 3 193643579 missense variant A/G snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1555817157
rs1555817157
ABHD12
16 0.742 0.280 20 25339320 frameshift variant TCTTCCTCAGGCG/- del 0.700 1.000 1 2018 2018
dbSNP: rs28939714
rs28939714
NDUFS3
3 0.882 0.160 11 47582140 missense variant C/G;T snv 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs74315205
rs74315205
WFS1 ; LOC107986257
7 0.807 0.360 4 6302385 missense variant G/A snv 0.010 1.000 1 2008 2008
dbSNP: rs746681765
rs746681765
SLC25A46
3 0.882 0.080 5 110761543 missense variant C/A;T snv 2.8E-05 0.010 1.000 1 2017 2017
dbSNP: rs80356524
rs80356524
OPA3
3 0.882 0.200 19 45553777 missense variant C/T snv 0.010 1.000 1 2010 2010
dbSNP: rs886037832
rs886037832
TWNK ; MRPL43
9 0.851 0.280 10 100988541 frameshift variant T/- delins 0.700 1.000 1 2016 2016
dbSNP: rs1020764190
rs1020764190
AFG3L2
2 0.925 0.120 18 12351330 missense variant G/A snv 0.700 0
dbSNP: rs1057518927
rs1057518927
OAT
4 0.925 0.080 10 124402952 missense variant T/C snv 0.700 0
dbSNP: rs1057519286
rs1057519286
MECR
3 0.882 0.080 1 29196234 stop gained A/C;G snv 0.700 0
dbSNP: rs1057519287
rs1057519287
MECR
3 0.882 0.080 1 29216612 frameshift variant TGAT/- delins 0.700 0
dbSNP: rs1184021143
rs1184021143
SLC25A46
2 0.925 0.080 5 110761295 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs1555303073
rs1555303073
COL4A1
6 0.851 0.120 13 110176912 missense variant C/T snv 0.700 0
dbSNP: rs1555968941
rs1555968941
CACNA1C
31 0.752 0.280 12 2653847 missense variant G/A;C snv 0.700 0
dbSNP: rs387906799
rs387906799
KIF1A
19 0.742 0.200 2 240788118 missense variant G/A snv 0.700 0
dbSNP: rs672601363
rs672601363
KIF1A
6 0.851 0.080 2 240788109 missense variant C/T snv 0.700 0
dbSNP: rs672601366
rs672601366
KIF1A
6 0.851 0.120 2 240786339 missense variant C/G snv 0.700 0
dbSNP: rs672601367
rs672601367
KIF1A
7 0.851 0.080 2 240785066 missense variant T/G snv 0.700 0
dbSNP: rs672601369
rs672601369
KIF1A
10 0.790 0.120 2 240783780 missense variant C/T snv 0.700 0