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rs863224115

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224115(A;T)
Make rs863224115(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position68036308
GeneNDUFS8
is asnp
is mentioned by
dbSNPrs863224115
ebirs863224115
HLIrs863224115
Exacrs863224115
Varsomers863224115
Maprs863224115
PheGenIrs863224115
hapmaprs863224115
1000 genomesrs863224115
hgdprs863224115
ensemblrs863224115
gopubmedrs863224115
geneviewrs863224115
scholarrs863224115
googlers863224115
pharmgkbrs863224115
gwascentralrs863224115
openSNPrs863224115
23andMers863224115
23andMe allrs863224115
SNP Nexus

SNPshotrs863224115
SNPdbers863224115
MSV3drs863224115
GWAS Ctlgrs863224115
Max Magnitude0
ClinVar
Risk rs863224115(T;T)
Alt rs863224115(T;T)
Reference rs863224115(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS8
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67803775A>T
CLNSRC
CLNACC RCV000197784.1,