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rs863224089

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224089(C;C)
Make rs863224089(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position41397058
GeneNDUFAF1
is asnp
is mentioned by
dbSNPrs863224089
ebirs863224089
HLIrs863224089
Exacrs863224089
Varsomers863224089
Maprs863224089
PheGenIrs863224089
hapmaprs863224089
1000 genomesrs863224089
hgdprs863224089
ensemblrs863224089
gopubmedrs863224089
geneviewrs863224089
scholarrs863224089
googlers863224089
pharmgkbrs863224089
gwascentralrs863224089
openSNPrs863224089
23andMers863224089
23andMe allrs863224089
SNP Nexus

SNPshotrs863224089
SNPdbers863224089
MSV3drs863224089
GWAS Ctlgrs863224089
Max Magnitude0
ClinVar
Risk rs863224089(C;C)
Alt rs863224089(C;C)
Reference rs863224089(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFAF1
CLNDBN not provided
Reversed 1
HGVS NC_000015.9:g.41689256A>G
CLNSRC
CLNACC RCV000199345.1,