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: rs121965055
rs121965055
OAT
1 10 124398061 stop gained C/A snv 4.0E-06 0.700 0
dbSNP: rs121965057
rs121965057
OAT
2 1.000 0.080 10 124402930 stop gained G/C snv 1.6E-05 2.8E-05 0.700 0
dbSNP: rs121965058
rs121965058
OAT
1 10 124397986 stop gained G/A snv 4.0E-06 0.700 0
dbSNP: rs121965060
rs121965060
OAT
2 1.000 0.080 10 124408897 missense variant G/C snv 0.700 0
dbSNP: rs1800456
rs1800456
OAT
2 1.000 0.080 10 124397951 missense variant C/A;G;T snv 2.8E-04; 4.0E-06 0.700 0
dbSNP: rs267606923
rs267606923
OAT
1 10 124405551 stop gained C/T snv 0.700 0
dbSNP: rs267606924
rs267606924
OAT
1 10 124403003 stop gained C/T snv 4.0E-06 0.700 0
dbSNP: rs267606925
rs267606925
OAT
2 1.000 0.080 10 124405488 missense variant G/T snv 8.0E-06 2.8E-05 0.700 0
dbSNP: rs386833595
rs386833595
OAT
1 10 124400881 missense variant C/T snv 0.700 0
dbSNP: rs386833596
rs386833596
OAT
1 10 124398090 stop gained C/T snv 7.0E-06 0.700 0
dbSNP: rs386833597
rs386833597
OAT
2 1.000 0.080 10 124398081 missense variant C/T snv 0.700 0
dbSNP: rs386833598
rs386833598
OAT
2 1.000 0.080 10 124397955 missense variant A/T snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs386833601
rs386833601
OAT
1 10 124411670 intron variant G/C snv 0.700 0
dbSNP: rs386833602
rs386833602
OAT
2 1.000 0.080 10 124408898 missense variant G/T snv 0.700 0
dbSNP: rs386833603
rs386833603
OAT
1 10 124408893 missense variant C/T snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs386833604
rs386833604
OAT
2 1.000 0.080 10 124408854 missense variant T/C snv 0.700 0
dbSNP: rs386833605
rs386833605
OAT
1 10 124408803 missense variant C/T snv 0.700 0
dbSNP: rs386833608
rs386833608
OAT
1 10 124408639 splice acceptor variant T/C snv 0.700 0
dbSNP: rs386833610
rs386833610
OAT
1 10 124408637 missense variant C/T snv 0.700 0
dbSNP: rs386833613
rs386833613
OAT
1 10 124405542 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs386833614
rs386833614
OAT
1 10 124405501 missense variant C/A snv 0.700 0
dbSNP: rs386833615
rs386833615
OAT
1 10 124403871 missense variant T/C snv 1.6E-05 7.0E-06 0.700 0
dbSNP: rs386833617
rs386833617
OAT
1 10 124403821 stop gained G/A;T snv 8.0E-06 0.700 0
dbSNP: rs386833618
rs386833618
OAT
2 1.000 0.080 10 124403027 missense variant G/A snv 4.4E-05 1.4E-05 0.700 0
dbSNP: rs386833619
rs386833619
OAT
1 10 124401841 splice acceptor variant T/C snv 0.700 0