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: rs587777659
rs587777659
ARMC5
1 1.000 16 31466773 missense variant C/T snv 0.800 1.000 10 2013 2018
dbSNP: rs587777661
rs587777661
ARMC5
1 1.000 16 31464666 missense variant T/C snv 0.800 1.000 10 2013 2018
dbSNP: rs587777662
rs587777662
ARMC5
1 1.000 16 31464800 missense variant C/T snv 4.4E-06 2.1E-05 0.800 1.000 10 2013 2018
dbSNP: rs587777663
rs587777663
ARMC5
1 1.000 16 31462641 missense variant T/C snv 0.800 1.000 10 2013 2018
dbSNP: rs1293014259
rs1293014259
ARMC5
1 1.000 16 31462499 missense variant C/G;T snv 8.1E-06 0.700 1.000 10 2013 2018
dbSNP: rs1385397608
rs1385397608
ARMC5
1 1.000 16 31462631 missense variant C/T snv 7.0E-06 0.700 1.000 10 2013 2018
dbSNP: rs200951744
rs200951744
ARMC5
1 1.000 16 31466273 missense variant C/G snv 1.7E-03 1.7E-03 0.700 1.000 10 2013 2018
dbSNP: rs35461188
rs35461188
ARMC5
1 1.000 16 31462515 missense variant G/C snv 1.1E-03 6.6E-04 0.700 1.000 10 2013 2018
dbSNP: rs114930262
rs114930262
ARMC5
1 1.000 16 31459990 missense variant C/G;T snv 1.7E-05; 1.6E-03 0.700 0
dbSNP: rs1415974570
rs1415974570
ARMC5
1 1.000 16 31462491 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs369721476
rs369721476
ARMC5
1 1.000 16 31462346 stop gained C/T snv 4.1E-06 7.0E-06 0.700 0
dbSNP: rs370836071
rs370836071
ARMC5
1 1.000 16 31465913 missense variant C/T snv 6.1E-05 5.6E-05 0.700 0
dbSNP: rs587777660
rs587777660
ARMC5
1 1.000 16 31459780 stop gained C/T snv 0.700 0