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rs797045055

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045055(A;G)
Make rs797045055(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeMT
Position14597
GeneMT-ND6
is asnp
is mentioned by
dbSNPrs797045055
ebirs797045055
HLIrs797045055
Exacrs797045055
Varsomers797045055
Maprs797045055
PheGenIrs797045055
hapmaprs797045055
1000 genomesrs797045055
hgdprs797045055
ensemblrs797045055
gopubmedrs797045055
geneviewrs797045055
scholarrs797045055
googlers797045055
pharmgkbrs797045055
gwascentralrs797045055
openSNPrs797045055
23andMers797045055
23andMe allrs797045055
SNP Nexus

SNPshotrs797045055
SNPdbers797045055
MSV3drs797045055
GWAS Ctlgrs797045055
Max Magnitude0
ClinVar
Risk rs797045055(G;G)
Alt rs797045055(G;G)
Reference rs797045055(A;A)
Significance Probable-Pathogenic
Disease Dysarthria Dystonia
Variation info
Gene ND6
CLNDBN Dysarthria Dystonia
Reversed 0
HGVS NC_012920.1:m.14597A>G
CLNSRC Baylor College of Medicine
CLNACC RCV000191107.1,