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rs34960210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs34960210(-;A)
Make rs34960210(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position95035578
GeneNDUFAF6
is asnp
is mentioned by
dbSNPrs34960210
ClinGenrs34960210
ebirs34960210
HLIrs34960210
Exacrs34960210
Varsomers34960210
Maprs34960210
PheGenIrs34960210
hapmaprs34960210
1000 genomesrs34960210
hgdprs34960210
ensemblrs34960210
gopubmedrs34960210
geneviewrs34960210
scholarrs34960210
googlers34960210
pharmgkbrs34960210
gwascentralrs34960210
openSNPrs34960210
23andMers34960210
23andMe allrs34960210
SNP Nexus

SNPshotrs34960210
SNPdbers34960210
MSV3drs34960210
GWAS Ctlgrs34960210
Max Magnitude0
ClinVar
Risk rs34960210(A;A) rs34960210(AA;AA) rs34960210(AAA;AAA) rs34960210(AAAA;AAAA) Rs34960210(T;T)
Alt rs34960210(A;A) rs34960210(AA;AA) rs34960210(AAA;AAA) rs34960210(AAAA;AAAA) Rs34960210(T;T)
Reference Rs34960210(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFAF6
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.96047806dupT
CLNSRC
CLNACC RCV000198813.1,