Gene: MCCC1 ×
Source: UNIPROT ×
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: rs119103212
rs119103212
MCCC1
1 0.925 0.120 3 183045522 missense variant A/C snv 1.6E-05 5.6E-05 0.800 1.000 0 2001 2015
dbSNP: rs119103213
rs119103213
MCCC1
1 1.000 0.120 3 183041679 missense variant T/G snv 1.3E-04 7.7E-05 0.800 1.000 0 2001 2015
dbSNP: rs1057520695
rs1057520695
MCCC1
1 1.000 0.120 3 183092514 missense variant G/C snv 0.700 1.000 11 2001 2016
dbSNP: rs186209189
rs186209189
MCCC1
1 1.000 0.120 3 183071223 missense variant C/A;T snv 4.0E-06; 8.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs199517715
rs199517715
MCCC1
1 1.000 0.120 3 183092545 missense variant C/T snv 4.0E-05 3.5E-05 0.700 1.000 11 2001 2016
dbSNP: rs201041864
rs201041864
MCCC1
1 1.000 0.120 3 183057312 missense variant G/A snv 1.4E-04 1.0E-04 0.700 1.000 11 2001 2016
dbSNP: rs201386261
rs201386261
MCCC1
1 1.000 0.120 3 183041738 missense variant C/T snv 2.4E-05 0.700 1.000 11 2001 2016
dbSNP: rs202197951
rs202197951
MCCC1
1 1.000 0.120 3 183072469 missense variant C/T snv 1.2E-05 2.1E-05 0.700 1.000 11 2001 2016
dbSNP: rs376289130
rs376289130
MCCC1
1 1.000 0.120 3 183039101 missense variant A/C;G snv 4.0E-05 1.1E-04 0.700 1.000 11 2001 2016
dbSNP: rs398124352
rs398124352
MCCC1
1 1.000 0.120 3 183039088 missense variant C/A;G;T snv 3.2E-05; 4.0E-06; 8.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs746500530
rs746500530
MCCC1
1 1.000 0.120 3 183057321 missense variant T/C snv 2.5E-05 1.4E-05 0.700 1.000 11 2001 2016
dbSNP: rs754437245
rs754437245
MCCC1
1 1.000 0.120 3 183057342 missense variant C/T snv 1.6E-05 7.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs755328329
rs755328329
MCCC1
1 1.000 0.120 3 183041719 missense variant T/G snv 4.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs768785753
rs768785753
MCCC1
1 1.000 0.120 3 183039072 missense variant C/T snv 2.8E-05 3.5E-05 0.700 1.000 11 2001 2016
dbSNP: rs119103214
rs119103214
MCCC1
1 1.000 0.120 3 183037218 missense variant C/G snv 0.700 0
dbSNP: rs119103215
rs119103215
MCCC1
1 1.000 0.120 3 183039093 missense variant A/G snv 0.700 0
dbSNP: rs119103216
rs119103216
MCCC1
1 1.000 0.120 3 183034068 missense variant G/A snv 0.700 0
dbSNP: rs119103218
rs119103218
MCCC1
1 1.000 0.120 3 183037432 missense variant A/C snv 0.700 0
dbSNP: rs1229069160
rs1229069160
MCCC1
1 1.000 0.120 3 183072457 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs1326114075
rs1326114075
MCCC1
1 1.000 0.120 3 183057318 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1333357031
rs1333357031
MCCC1
1 1.000 0.120 3 183041687 missense variant C/T snv 1.4E-05 0.700 0
dbSNP: rs727504004
rs727504004
MCCC1
1 1.000 0.120 3 183071066 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs748201122
rs748201122
MCCC1
1 1.000 0.120 3 183071310 missense variant C/A;T snv 4.0E-06 0.700 0
dbSNP: rs757362635
rs757362635
MCCC1
1 1.000 0.120 3 183071290 missense variant A/G;T snv 2.4E-05; 1.2E-05 0.700 0
dbSNP: rs773433541
rs773433541
MCCC1
1 1.000 0.120 3 183057358 missense variant A/C;G snv 8.1E-06 0.700 0