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rs200890363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs200890363(A;G)
Make rs200890363(G;G)
ReferenceGRCh38 38.1/141
ChromosomeMT
Position12397
GeneMT-ND4
is asnp
is mentioned by
dbSNPrs200890363
ebirs200890363
HLIrs200890363
Exacrs200890363
Varsomers200890363
Maprs200890363
PheGenIrs200890363
hapmaprs200890363
1000 genomesrs200890363
hgdprs200890363
ensemblrs200890363
gopubmedrs200890363
geneviewrs200890363
scholarrs200890363
googlers200890363
pharmgkbrs200890363
gwascentralrs200890363
openSNPrs200890363
23andMers200890363
23andMe allrs200890363
SNP Nexus

SNPshotrs200890363
SNPdbers200890363
MSV3drs200890363
GWAS Ctlgrs200890363
GMAF0.003742
Max Magnitude0
ClinVar
Risk rs200890363(G;G)
Alt rs200890363(G;G)
Reference rs200890363(A;A)
Significance Other
Disease Parkinson disease 6
Variation info
Gene ND5
CLNDBN Parkinson disease 6, autosomal recessive early-onset
Reversed 0
HGVS NC_012920.1:m.12397A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010351.3,