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rs119103221

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119103221(C;G)
Make rs119103221(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position71635176
GeneMCCC2
is asnp
is mentioned by
dbSNPrs119103221
ebirs119103221
HLIrs119103221
Exacrs119103221
Varsomers119103221
Maprs119103221
PheGenIrs119103221
hapmaprs119103221
1000 genomesrs119103221
hgdprs119103221
ensemblrs119103221
gopubmedrs119103221
geneviewrs119103221
scholarrs119103221
googlers119103221
pharmgkbrs119103221
gwascentralrs119103221
openSNPrs119103221
23andMers119103221
23andMe allrs119103221
SNP Nexus

SNPshotrs119103221
SNPdbers119103221
MSV3drs119103221
GWAS Ctlgrs119103221
Max Magnitude0
OMIM609014
Desc
Variant0004
Relatedalso
ClinVar
Risk rs119103221(G;G)
Alt rs119103221(G;G)
Reference rs119103221(C;C)
Significance Pathogenic
Disease 3-methylcrotonyl CoA carboxylase 2 deficiency not provided
Variation info
Gene MCCC2
CLNDBN 3-methylcrotonyl CoA carboxylase 2 deficiency not provided
Reversed 0
HGVS NC_000005.9:g.70931003C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000001999.3, RCV000186001.1,