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rs863224113

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224113(C;C)
Make rs863224113(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position1383928
GeneNDUFS7
is asnp
is mentioned by
dbSNPrs863224113
ebirs863224113
HLIrs863224113
Exacrs863224113
Varsomers863224113
Maprs863224113
PheGenIrs863224113
hapmaprs863224113
1000 genomesrs863224113
hgdprs863224113
ensemblrs863224113
gopubmedrs863224113
geneviewrs863224113
scholarrs863224113
googlers863224113
pharmgkbrs863224113
gwascentralrs863224113
openSNPrs863224113
23andMers863224113
23andMe allrs863224113
SNP Nexus

SNPshotrs863224113
SNPdbers863224113
MSV3drs863224113
GWAS Ctlgrs863224113
Max Magnitude0
ClinVar
Risk rs863224113(C;C)
Alt rs863224113(C;C)
Reference rs863224113(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFS7
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.1383927T>C
CLNSRC
CLNACC RCV000198353.1,