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rs863224111

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224111(A;T)
Make rs863224111(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position1814457
GeneNDUFS6
is asnp
is mentioned by
dbSNPrs863224111
ebirs863224111
HLIrs863224111
Exacrs863224111
Varsomers863224111
Maprs863224111
PheGenIrs863224111
hapmaprs863224111
1000 genomesrs863224111
hgdprs863224111
ensemblrs863224111
gopubmedrs863224111
geneviewrs863224111
scholarrs863224111
googlers863224111
pharmgkbrs863224111
gwascentralrs863224111
openSNPrs863224111
23andMers863224111
23andMe allrs863224111
SNP Nexus

SNPshotrs863224111
SNPdbers863224111
MSV3drs863224111
GWAS Ctlgrs863224111
Max Magnitude0
ClinVar
Risk rs863224111(T;T)
Alt rs863224111(T;T)
Reference rs863224111(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS6
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.1814571A>T
CLNSRC
CLNACC RCV000196437.1,