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: rs141970897
rs141970897
CRAT
8 0.925 0.200 9 129104269 missense variant T/C snv 1.1E-03 7.8E-04 0.700 1.000 1 2020 2020
dbSNP: rs374997012
rs374997012
TWNK ; MRPL43
9 0.851 0.280 10 100989114 missense variant C/T snv 8.0E-06 7.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs762425351
rs762425351
CRAT
8 0.925 0.200 9 129095573 missense variant C/T snv 1.2E-04 7.7E-05 0.700 1.000 1 2020 2020
dbSNP: rs886037832
rs886037832
TWNK ; MRPL43
9 0.851 0.280 10 100988541 frameshift variant T/- delins 0.700 1.000 1 2016 2016
dbSNP: rs1345176461
rs1345176461
IRF2BPL ; LOC107984638
40 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 0.700 0
dbSNP: rs1448259271
rs1448259271
IRF2BPL ; LOC107984638
23 0.790 0.240 14 77027279 stop gained C/A;T snv 0.700 0
dbSNP: rs781939614
rs781939614
PEX11B
11 0.851 0.240 1 145916914 stop gained G/A snv 4.0E-06 0.700 0
dbSNP: rs781984979
rs781984979
PEX11B
11 0.851 0.240 1 145912346 stop gained G/A snv 4.0E-06 0.700 0
dbSNP: rs121434589
rs121434589
MYH2 ; MYHAS
8 0.851 0.200 17 10535137 missense variant C/T snv 0.010 1.000 1 2015 2015
dbSNP: rs267606799
rs267606799
FBN1
2 1.000 0.120 15 48467975 missense variant C/A;G snv 0.010 1.000 1 2016 2016
dbSNP: rs786201023
rs786201023
MYH2 ; MYHAS
3 1.000 0.160 17 10523154 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs80356529
rs80356529
OPA1
9 0.827 0.240 3 193643996 missense variant G/A;C snv 0.010 1.000 1 2005 2005