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rs906807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs906807(A;G)
Make rs906807(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position9117869
GeneNDUFV2
is asnp
is mentioned by
dbSNPrs906807
ebirs906807
HLIrs906807
Exacrs906807
Varsomers906807
Maprs906807
PheGenIrs906807
hapmaprs906807
1000 genomesrs906807
hgdprs906807
ensemblrs906807
gopubmedrs906807
geneviewrs906807
scholarrs906807
googlers906807
pharmgkbrs906807
gwascentralrs906807
openSNPrs906807
23andMers906807
23andMe allrs906807
SNP Nexus

SNPshotrs906807
SNPdbers906807
MSV3drs906807
GWAS Ctlgrs906807
GMAF0.2406
Max Magnitude0
? (A;A) (A;G) (G;G) 28
OMIM600532
DescPARKINSON DISEASE, SUSCEPTIBILITY TO
Variant0001
Relatedalso


[PMID 19194776] Association study on the mitochondrial gene NDUFV2 and bipolar disorder in the Chinese Han population


ClinVar
Risk rs906807(G;G)
Alt rs906807(G;G)
Reference rs906807(A;A)
Significance Other
Disease Parkinson disease not specified
Variation info
Gene NDUFV2
CLNDBN Parkinson disease, mitochondrial not specified
Reversed 1
HGVS NC_000018.9:g.9117867T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000009621.2, RCV000117718.3,



[PMID 16436204OA-icon.png] GPNN: power studies and applications of a neural network method for detecting gene-gene interactions in studies of human disease.


[PMID 17601350OA-icon.png] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.


GET Evidence
NDUFV2-V29A
aa_change Val29Ala
aa_change_short V29A
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.799107
summary