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rs119103212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs119103212(G;G)
Make rs119103212(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position183045522
GeneMCCC1
is asnp
is mentioned by
dbSNPrs119103212
dbSNP (old)rs119103212
ClinGenrs119103212
ebirs119103212
HLIrs119103212
Exacrs119103212
Gnomadrs119103212
Varsomers119103212
Maprs119103212
PheGenIrs119103212
Biobankrs119103212
1000 genomesrs119103212
hgdprs119103212
ensemblrs119103212
gopubmedrs119103212
geneviewrs119103212
scholarrs119103212
googlers119103212
pharmgkbrs119103212
gwascentralrs119103212
openSNPrs119103212
23andMers119103212
23andMe allrs119103212
SNP Nexus

SNPshotrs119103212
SNPdbers119103212
MSV3drs119103212
GWAS Ctlgrs119103212
Max Magnitude0
OMIM609010
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119103212(G;G)
Alt rs119103212(G;G)
Reference Rs119103212(T;T)
Significance Other
Disease 3 Methylcrotonyl-CoA carboxylase 1 deficiency not provided
Variation info
Gene MCCC1
CLNDBN 3 Methylcrotonyl-CoA carboxylase 1 deficiency not provided
Reversed 1
HGVS NC_000003.11:g.182763310A>C
CLNSRC HGMD OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000002006.4, RCV000081995.4,