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

rs199474671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199474671(A;A)
Make rs199474671(A;G)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position5549
GeneSMR3B
is asnp
is mentioned by
dbSNPrs199474671
ebirs199474671
HLIrs199474671
Exacrs199474671
Varsomers199474671
Maprs199474671
PheGenIrs199474671
hapmaprs199474671
1000 genomesrs199474671
hgdprs199474671
ensemblrs199474671
gopubmedrs199474671
geneviewrs199474671
scholarrs199474671
googlers199474671
pharmgkbrs199474671
gwascentralrs199474671
openSNPrs199474671
23andMers199474671
23andMe allrs199474671
SNP Nexus

SNPshotrs199474671
SNPdbers199474671
MSV3drs199474671
GWAS Ctlgrs199474671
Max Magnitude0
ClinVar
Risk rs199474671(A;A)
Alt rs199474671(A;A)
Reference rs199474671(G;G)
Significance Pathogenic
Disease Encephalopathy
Variation info
Gene
CLNDBN Encephalopathy, mitochondrial
Reversed 0
HGVS NC_012920.1:m.5549G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010163.2,