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rs863224079

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224079(A;G)
Make rs863224079(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position5894856
GeneNDUFA11
is asnp
is mentioned by
dbSNPrs863224079
ebirs863224079
HLIrs863224079
Exacrs863224079
Varsomers863224079
Maprs863224079
PheGenIrs863224079
hapmaprs863224079
1000 genomesrs863224079
hgdprs863224079
ensemblrs863224079
gopubmedrs863224079
geneviewrs863224079
scholarrs863224079
googlers863224079
pharmgkbrs863224079
gwascentralrs863224079
openSNPrs863224079
23andMers863224079
23andMe allrs863224079
SNP Nexus

SNPshotrs863224079
SNPdbers863224079
MSV3drs863224079
GWAS Ctlgrs863224079
Max Magnitude0
ClinVar
Risk rs863224079(G;G)
Alt rs863224079(G;G)
Reference rs863224079(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFA11
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.5894867T>C
CLNSRC
CLNACC RCV000195679.2,