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rs104893849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893849(A;G)
Make rs104893849(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position145646043
GeneMMAA
is asnp
is mentioned by
dbSNPrs104893849
ebirs104893849
HLIrs104893849
Exacrs104893849
Varsomers104893849
Maprs104893849
PheGenIrs104893849
hapmaprs104893849
1000 genomesrs104893849
hgdprs104893849
ensemblrs104893849
gopubmedrs104893849
geneviewrs104893849
scholarrs104893849
googlers104893849
pharmgkbrs104893849
gwascentralrs104893849
openSNPrs104893849
23andMers104893849
23andMe allrs104893849
SNP Nexus

SNPshotrs104893849
SNPdbers104893849
MSV3drs104893849
GWAS Ctlgrs104893849
Max Magnitude0
OMIM607481
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104893849(G;G)
Alt rs104893849(G;G)
Reference rs104893849(A;A)
Significance Pathogenic
Disease Methylmalonic aciduria cblA type
Variation info
Gene MMAA
CLNDBN Methylmalonic aciduria cblA type
Reversed 0
HGVS NC_000004.11:g.146567195A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003309.2,