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: rs724160026
rs724160026
AIFM1 ; RAB33A
2 0.925 0.160 X 130136729 missense variant C/G snv 0.800 1.000 1 2015 2015
dbSNP: rs863225431
rs863225431
AIFM1 ; RAB33A
2 0.925 0.160 X 130133409 missense variant C/T snv 0.800 1.000 1 2015 2015
dbSNP: rs863225432
rs863225432
AIFM1 ; RAB33A
1 1.000 0.160 X 130140536 missense variant T/C snv 0.800 1.000 1 2015 2015
dbSNP: rs724160020
rs724160020
AIFM1 ; RAB33A
1 1.000 0.160 X 130136086 missense variant G/A snv 0.800 0
dbSNP: rs724160021
rs724160021
AIFM1 ; RAB33A
2 0.925 0.160 X 130136085 missense variant C/T snv 0.800 0
dbSNP: rs724160022
rs724160022
AIFM1 ; RAB33A
2 0.925 0.160 X 130133337 missense variant G/A snv 0.800 0
dbSNP: rs724160023
rs724160023
AIFM1 ; RAB33A
2 0.925 0.160 X 130131756 missense variant C/T snv 5.5E-06 0.800 0
dbSNP: rs1223488720
rs1223488720
AIFM1 ; RAB33A
1 1.000 0.160 X 130136062 missense variant G/A snv 9.5E-06 0.700 1.000 1 2015 2015
dbSNP: rs184474885
rs184474885
AIFM1 ; RAB33A
2 0.925 0.160 X 130137123 missense variant G/A snv 1.9E-04 3.8E-05 0.700 1.000 1 2015 2015
dbSNP: rs724160014
rs724160014
AIFM1 ; RAB33A
1 1.000 0.160 X 130165779 5 prime UTR variant C/A;G snv 0.700 0
dbSNP: rs724160015
rs724160015
AIFM1 ; RAB33A
2 0.925 0.160 X 130147792 missense variant G/A snv 0.700 0
dbSNP: rs724160016
rs724160016
AIFM1 ; RAB33A
2 0.925 0.160 X 130147525 missense variant CA/AG mnv 0.700 0
dbSNP: rs724160017
rs724160017
AIFM1 ; RAB33A
2 0.925 0.160 X 130139808 missense variant G/A snv 2.2E-05 9.5E-06 0.700 0
dbSNP: rs724160018
rs724160018
AIFM1 ; RAB33A
2 0.925 0.160 X 130138700 missense variant A/G snv 0.700 0
dbSNP: rs724160019
rs724160019
AIFM1 ; RAB33A
1 1.000 0.160 X 130136710 missense variant T/C snv 3.8E-05 1.9E-05 0.700 0
dbSNP: rs724160024
rs724160024
AIFM1 ; RAB33A
1 1.000 0.160 X 130130062 missense variant A/G snv 0.700 0
dbSNP: rs724160025
rs724160025
AIFM1 ; RAB33A
2 0.925 0.160 X 130133442 missense variant G/A snv 0.700 0