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

rs544349961

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs544349961(A;A)
Make rs544349961(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position183041720
GeneMCCC1
is asnp
is mentioned by
dbSNPrs544349961
ebirs544349961
HLIrs544349961
Exacrs544349961
Varsomers544349961
Maprs544349961
PheGenIrs544349961
hapmaprs544349961
1000 genomesrs544349961
hgdprs544349961
ensemblrs544349961
gopubmedrs544349961
geneviewrs544349961
scholarrs544349961
googlers544349961
pharmgkbrs544349961
gwascentralrs544349961
openSNPrs544349961
23andMers544349961
23andMe allrs544349961
SNP Nexus

SNPshotrs544349961
SNPdbers544349961
MSV3drs544349961
GWAS Ctlgrs544349961
Max Magnitude0
ClinVar
Risk rs544349961(A;A)
Alt rs544349961(A;A)
Reference rs544349961(G;G)
Significance Pathogenic
Disease 3 Methylcrotonyl-CoA carboxylase 1 deficiency not provided
Variation info
Gene MCCC1
CLNDBN 3 Methylcrotonyl-CoA carboxylase 1 deficiency not provided
Reversed 0
HGVS NC_000003.11:g.182759508G>A
CLNSRC
CLNACC RCV000174145.1, RCV000185990.1,