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rs765373403

From SNPedia

Orientationplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
Make rs765373403(-;-)
Make rs765373403(-;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position49453628
GeneMUT
is asnp
is mentioned by
dbSNPrs765373403
ebirs765373403
HLIrs765373403
Exacrs765373403
Varsomers765373403
Maprs765373403
PheGenIrs765373403
hapmaprs765373403
1000 genomesrs765373403
hgdprs765373403
ensemblrs765373403
gopubmedrs765373403
geneviewrs765373403
scholarrs765373403
googlers765373403
pharmgkbrs765373403
gwascentralrs765373403
openSNPrs765373403
23andMers765373403
23andMe allrs765373403
SNP Nexus

SNPshotrs765373403
SNPdbers765373403
MSV3drs765373403
GWAS Ctlgrs765373403
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs765373403(AGA;AGA)
Significance Pathogenic
Disease Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Variation info
Gene MUT
CLNDBN Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
Reversed 0
HGVS NC_000006.11:g.49421341_49421343delAGA
CLNSRC
CLNACC RCV000210826.1,