Have questions? Visit https://www.reddit.com/r/SNPedia

rs773774134

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773774134(C;T)
Make rs773774134(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
is asnp
is mentioned by
dbSNPrs773774134
ebirs773774134
HLIrs773774134
Exacrs773774134
Varsomers773774134
Maprs773774134
PheGenIrs773774134
hapmaprs773774134
1000 genomesrs773774134
hgdprs773774134
ensemblrs773774134
gopubmedrs773774134
geneviewrs773774134
scholarrs773774134
googlers773774134
pharmgkbrs773774134
gwascentralrs773774134
openSNPrs773774134
23andMers773774134
23andMe allrs773774134
SNP Nexus

SNPshotrs773774134
SNPdbers773774134
MSV3drs773774134
GWAS Ctlgrs773774134
Max Magnitude0
ClinVar
Risk rs773774134(T;T)
Alt rs773774134(T;T)
Reference rs773774134(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.70900239C>T
CLNSRC
CLNACC RCV000179523.1, RCV000185999.1,