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: rs119103226
rs119103226
MCCC2
1 1.000 0.120 5 71634977 missense variant G/T snv 5.6E-05 7.0E-06 0.800 1.000 13 2001 2016
dbSNP: rs150591260
rs150591260
MCCC2
1 1.000 0.120 5 71641018 missense variant G/A;C snv 7.8E-04; 4.0E-06 5.7E-04 0.800 1.000 13 2001 2016
dbSNP: rs148773718
rs148773718
MCCC2
1 1.000 0.120 5 71650118 missense variant G/A snv 9.5E-05 1.5E-04 0.800 1.000 11 2001 2016
dbSNP: rs141030969
rs141030969
MCCC2
1 1.000 0.120 5 71602585 missense variant C/T snv 4.4E-05 2.1E-05 0.800 1.000 2 2005 2012
dbSNP: rs757052602
rs757052602
MCCC2
1 1.000 0.120 5 71641068 missense variant A/T snv 3.6E-04 1.1E-04 0.800 1.000 2 2011 2015
dbSNP: rs766753795
rs766753795
MCCC2
1 1.000 0.120 5 71626703 missense variant A/G snv 0.800 1.000 1 2016 2016
dbSNP: rs773774134
rs773774134
MCCC2
1 1.000 0.120 5 71604412 missense variant C/T snv 1.6E-05 2.1E-05 0.800 1.000 1 2005 2005
dbSNP: rs119103219
rs119103219
MCCC2
1 1.000 0.120 5 71599672 missense variant G/A;C snv 3.6E-05 1.4E-04 0.800 0
dbSNP: rs119103220
rs119103220
MCCC2
1 1.000 0.120 5 71602586 missense variant G/A snv 7.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs119103221
rs119103221
MCCC2
1 1.000 0.120 5 71635176 missense variant C/G snv 4.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs119103222
rs119103222
MCCC2
1 1.000 0.120 5 71602621 missense variant T/C snv 4.0E-06 7.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs119103223
rs119103223
MCCC2
1 1.000 0.120 5 71632185 missense variant G/C snv 0.700 1.000 11 2001 2016
dbSNP: rs119103224
rs119103224
MCCC2
1 1.000 0.120 5 71649189 missense variant A/G;T snv 2.0E-05; 8.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs119103225
rs119103225
MCCC2
1 1.000 0.120 5 71604413 missense variant A/G snv 0.700 1.000 11 2001 2016
dbSNP: rs1257849672
rs1257849672
MCCC2
1 1.000 0.120 5 71656831 missense variant A/G snv 4.0E-06 3.5E-05 0.700 1.000 11 2001 2016
dbSNP: rs139852818
rs139852818
MCCC2
1 1.000 0.120 5 71649202 missense variant T/A;C snv 4.0E-06; 1.0E-03 0.700 1.000 11 2001 2016
dbSNP: rs140806722
rs140806722
MCCC2
1 1.000 0.120 5 71604443 missense variant T/A snv 2.1E-03 2.6E-03 0.700 1.000 11 2001 2016
dbSNP: rs142887940
rs142887940
MCCC2
1 1.000 0.120 5 71646269 missense variant A/C;G snv 4.0E-06; 1.1E-04 0.700 1.000 11 2001 2016
dbSNP: rs1443551700
rs1443551700
MCCC2
1 1.000 0.120 5 71635202 missense variant G/A snv 4.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs1450515408
rs1450515408
MCCC2
1 1.000 0.120 5 71646220 missense variant T/G snv 0.700 1.000 11 2001 2016
dbSNP: rs1459143051
rs1459143051
MCCC2
1 1.000 0.120 5 71652747 missense variant A/G snv 0.700 1.000 11 2001 2016
dbSNP: rs150327768
rs150327768
MCCC2
1 1.000 0.120 5 71652739 missense variant A/C;G;T snv 2.0E-05; 8.0E-06; 4.0E-06 0.700 1.000 11 2001 2016
dbSNP: rs1554134065
rs1554134065
MCCC2
1 1.000 0.120 5 71602577 missense variant A/C snv 0.700 1.000 11 2001 2016
dbSNP: rs277995
rs277995
MCCC2
1 1.000 0.120 5 71626656 missense variant G/C snv 2.8E-05 4.9E-05 0.700 1.000 11 2001 2016
dbSNP: rs535519604
rs535519604
MCCC2
1 1.000 0.120 5 71604422 missense variant G/A;T snv 4.0E-06; 4.0E-06 0.700 1.000 11 2001 2016