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rs772395858

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs772395858(C;C)
Make rs772395858(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position183071122
GeneMCCC1
is asnp
is mentioned by
dbSNPrs772395858
ebirs772395858
HLIrs772395858
Exacrs772395858
Varsomers772395858
Maprs772395858
PheGenIrs772395858
hapmaprs772395858
1000 genomesrs772395858
hgdprs772395858
ensemblrs772395858
gopubmedrs772395858
geneviewrs772395858
scholarrs772395858
googlers772395858
pharmgkbrs772395858
gwascentralrs772395858
openSNPrs772395858
23andMers772395858
23andMe allrs772395858
SNP Nexus

SNPshotrs772395858
SNPdbers772395858
MSV3drs772395858
GWAS Ctlgrs772395858
Max Magnitude0
ClinVar
Risk rs772395858(C;C)
Alt rs772395858(C;C)
Reference rs772395858(T;T)
Significance Pathogenic
Disease 3 Methylcrotonyl-CoA carboxylase 1 deficiency
Variation info
Gene MCCC1
CLNDBN 3 Methylcrotonyl-CoA carboxylase 1 deficiency
Reversed 0
HGVS NC_000003.11:g.182788910T>C
CLNSRC
CLNACC RCV000179961.1,