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rs786200951

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786200951(A;A)
Make rs786200951(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position5610
is asnp
is mentioned by
dbSNPrs786200951
ebirs786200951
HLIrs786200951
Exacrs786200951
Varsomers786200951
Maprs786200951
PheGenIrs786200951
hapmaprs786200951
1000 genomesrs786200951
hgdprs786200951
ensemblrs786200951
gopubmedrs786200951
geneviewrs786200951
scholarrs786200951
googlers786200951
pharmgkbrs786200951
gwascentralrs786200951
openSNPrs786200951
23andMers786200951
23andMe allrs786200951
SNP Nexus

SNPshotrs786200951
SNPdbers786200951
MSV3drs786200951
GWAS Ctlgrs786200951
Max Magnitude0
ClinVar
Risk rs786200951(A;A)
Alt rs786200951(A;A)
Reference rs786200951(G;G)
Significance Pathogenic
Disease Mitochondrial myopathy
Variation info
Gene
CLNDBN Mitochondrial myopathy
Reversed 0
HGVS NC_012920.1:m.5610G>A
CLNSRC
CLNACC RCV000169781.1,