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rs1057516072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516072(A;A)
Make rs1057516072(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position15060
GeneCYTB
is asnp
is mentioned by
dbSNPrs1057516072
dbSNP (old)rs1057516072
ClinGenrs1057516072
ebirs1057516072
HLIrs1057516072
Exacrs1057516072
Gnomadrs1057516072
Varsomers1057516072
Maprs1057516072
PheGenIrs1057516072
Biobankrs1057516072
1000 genomesrs1057516072
hgdprs1057516072
ensemblrs1057516072
gopubmedrs1057516072
geneviewrs1057516072
scholarrs1057516072
googlers1057516072
pharmgkbrs1057516072
gwascentralrs1057516072
openSNPrs1057516072
23andMers1057516072
23andMe allrs1057516072
SNPshotrs1057516072
SNPdbers1057516072
MSV3drs1057516072
GWAS Ctlgrs1057516072
Max Magnitude0
ClinVar
Risk rs1057516072(A;A)
Alt rs1057516072(A;A)
Reference Rs1057516072(G;G)
Significance Probable-Pathogenic
Disease Bilateral lesions of basal ganglia Seizure Disorders
Variation info
Gene CYTB
CLNDBN Bilateral lesions of basal ganglia Seizure Disorders
Reversed 0
HGVS NC_012920.1:m.15060G>A
CLNSRC
CLNACC RCV000408920.1,