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rs199476110

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199476110(C;C)
Make rs199476110(C;T)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position14319
GeneMT-CYB
is asnp
is mentioned by
dbSNPrs199476110
ebirs199476110
HLIrs199476110
Exacrs199476110
Varsomers199476110
Maprs199476110
PheGenIrs199476110
hapmaprs199476110
1000 genomesrs199476110
hgdprs199476110
ensemblrs199476110
gopubmedrs199476110
geneviewrs199476110
scholarrs199476110
googlers199476110
pharmgkbrs199476110
gwascentralrs199476110
openSNPrs199476110
23andMers199476110
23andMe allrs199476110
SNP Nexus

SNPshotrs199476110
SNPdbers199476110
MSV3drs199476110
GWAS Ctlgrs199476110
GMAF0.001871
Max Magnitude0
ClinVar
Risk rs199476110(C;C)
Alt rs199476110(C;C)
Reference rs199476110(T;T)
Significance Other
Disease Parkinson disease 6
Variation info
Gene ND6
CLNDBN Parkinson disease 6, autosomal recessive early-onset
Reversed 0
HGVS NC_012920.1:m.14319T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010335.3,