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rs104893846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893846(C;T)
Make rs104893846(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position145639422
GeneMMAA
is asnp
is mentioned by
dbSNPrs104893846
ebirs104893846
HLIrs104893846
Exacrs104893846
Varsomers104893846
Maprs104893846
PheGenIrs104893846
hapmaprs104893846
1000 genomesrs104893846
hgdprs104893846
ensemblrs104893846
gopubmedrs104893846
geneviewrs104893846
scholarrs104893846
googlers104893846
pharmgkbrs104893846
gwascentralrs104893846
openSNPrs104893846
23andMers104893846
23andMe allrs104893846
SNP Nexus

SNPshotrs104893846
SNPdbers104893846
MSV3drs104893846
GWAS Ctlgrs104893846
Max Magnitude0
OMIM607481
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104893846(T;T)
Alt rs104893846(T;T)
Reference Rs104893846(C;C)
Significance Pathogenic
Disease Methylmalonic aciduria cblA type
Variation info
Gene MMAA
CLNDBN Methylmalonic aciduria cblA type
Reversed 0
HGVS NC_000004.11:g.146560574C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003308.2,