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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.p7 38.3/150
ChromosomeMT
Position14319
GeneND6
is asnp
is mentioned by
dbSNPrs199476110
dbSNP (classic)rs199476110
ClinGenrs199476110
ebirs199476110
HLIrs199476110
Exacrs199476110
Gnomadrs199476110
Varsomers199476110
LitVarrs199476110
Maprs199476110
PheGenIrs199476110
Biobankrs199476110
1000 genomesrs199476110
hgdprs199476110
ensemblrs199476110
geneviewrs199476110
scholarrs199476110
googlers199476110
pharmgkbrs199476110
gwascentralrs199476110
openSNPrs199476110
23andMers199476110
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,