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rs863224110

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224110(C;T)
Make rs863224110(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position1814399
GeneNDUFS6
is asnp
is mentioned by
dbSNPrs863224110
ebirs863224110
HLIrs863224110
Exacrs863224110
Varsomers863224110
Maprs863224110
PheGenIrs863224110
hapmaprs863224110
1000 genomesrs863224110
hgdprs863224110
ensemblrs863224110
gopubmedrs863224110
geneviewrs863224110
scholarrs863224110
googlers863224110
pharmgkbrs863224110
gwascentralrs863224110
openSNPrs863224110
23andMers863224110
23andMe allrs863224110
SNP Nexus

SNPshotrs863224110
SNPdbers863224110
MSV3drs863224110
GWAS Ctlgrs863224110
Max Magnitude0
ClinVar
Risk rs863224110(T;T)
Alt rs863224110(T;T)
Reference rs863224110(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS6
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.1814513C>T
CLNSRC
CLNACC RCV000199698.2,