Gene: MCCC2 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103219
rs119103219
MCCC2
0.800 GeneticVariation UNIPROT

dbSNP: rs141030969
rs141030969
MCCC2
0.800 GeneticVariation UNIPROT

dbSNP: rs757052602
rs757052602
MCCC2
0.800 GeneticVariation UNIPROT

dbSNP: rs766753795
rs766753795
MCCC2
0.800 GeneticVariation UNIPROT

dbSNP: rs773774134
rs773774134
MCCC2
0.800 GeneticVariation UNIPROT

dbSNP: rs1187203558
rs1187203558
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs1195601465
rs1195601465
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs1254750166
rs1254750166
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs398124370
rs398124370
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs398124371
rs398124371
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs727504011
rs727504011
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs748028684
rs748028684
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs758506791
rs758506791
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs765438239
rs765438239
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs773115035
rs773115035
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs774241918
rs774241918
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs886043524
rs886043524
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs979584886
rs979584886
MCCC2
0.700 GeneticVariation UNIPROT

dbSNP: rs119103226
rs119103226
MCCC2
0.800 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs148773718
rs148773718
MCCC2
0.800 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs150591260
rs150591260
MCCC2
0.800 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs119103220
rs119103220
MCCC2
0.700 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs119103221
rs119103221
MCCC2
0.700 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs119103222
rs119103222
MCCC2
0.700 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001
dbSNP: rs119103223
rs119103223
MCCC2
0.700 GeneticVariation UNIPROT The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism. 11170888

2001