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rs199476120

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199476120(A;G)
Make rs199476120(G;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position3397
GeneMT-ND1
is asnp
is mentioned by
dbSNPrs199476120
ebirs199476120
HLIrs199476120
Exacrs199476120
Varsomers199476120
Maprs199476120
PheGenIrs199476120
hapmaprs199476120
1000 genomesrs199476120
hgdprs199476120
ensemblrs199476120
gopubmedrs199476120
geneviewrs199476120
scholarrs199476120
googlers199476120
pharmgkbrs199476120
gwascentralrs199476120
openSNPrs199476120
23andMers199476120
23andMe allrs199476120
SNP Nexus

SNPshotrs199476120
SNPdbers199476120
MSV3drs199476120
GWAS Ctlgrs199476120
GMAF0.0009355
Max Magnitude0
ClinVar
Risk rs199476120(G;G)
Alt rs199476120(G;G)
Reference rs199476120(A;A)
Significance Pathogenic
Disease Alzheimer's disease Parkinson disease
Variation info
Gene ND1
CLNDBN Alzheimer's disease Parkinson disease, late-onset
Reversed 0
HGVS NC_012920.1:m.3397A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010376.3, RCV000010377.2,