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: rs62637027
rs62637027
NYX
1 1.000 0.080 X 41474012 missense variant GC/AA mnv 0.800 1.000 2 2000 2000
dbSNP: rs62637020
rs62637020
NYX
1 1.000 0.080 X 41473545 missense variant G/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637023
rs62637023
NYX
1 1.000 0.080 X 41473880 missense variant G/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637024
rs62637024
NYX
1 1.000 0.080 X 41473905 missense variant C/T snv 0.700 1.000 2 2000 2000
dbSNP: rs62637025
rs62637025
NYX
1 1.000 0.080 X 41473977 missense variant C/G snv 0.700 1.000 2 2000 2000
dbSNP: rs62637026
rs62637026
NYX
1 1.000 0.080 X 41474004 missense variant T/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637028
rs62637028
NYX
1 1.000 0.080 X 41474091 missense variant T/A snv 0.700 1.000 2 2000 2000
dbSNP: rs62637030
rs62637030
NYX
1 1.000 0.080 X 41474148 missense variant T/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637032
rs62637032
NYX
1 1.000 0.080 X 41474245 missense variant C/G;T snv 6.4E-06 0.700 1.000 2 2000 2000
dbSNP: rs62637033
rs62637033
NYX
1 1.000 0.080 X 41474307 missense variant T/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637034
rs62637034
NYX
1 1.000 0.080 X 41474346 missense variant T/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637035
rs62637035
NYX
1 1.000 0.080 X 41474388 missense variant A/G snv 0.700 1.000 2 2000 2000
dbSNP: rs62637036
rs62637036
NYX
1 1.000 0.080 X 41474493 missense variant T/C snv 0.700 1.000 2 2000 2000
dbSNP: rs62637038
rs62637038
NYX
1 1.000 0.080 X 41474562 missense variant G/T snv 0.700 1.000 2 2000 2000
dbSNP: rs104894910
rs104894910
NYX
3 0.882 0.080 X 41473734 missense variant G/C snv 0.700 0
dbSNP: rs104894911
rs104894911
NYX
1 1.000 0.080 X 41473755 missense variant T/C snv 0.700 0
dbSNP: rs62637021
rs62637021
NYX
1 1.000 0.080 X 41473558 stop gained C/A snv 0.700 0
dbSNP: rs62637037
rs62637037
NYX
1 1.000 0.080 X 41474502 stop gained G/A snv 1.2E-05 9.4E-05 0.700 0