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rs863224098

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224098(A;A)
Make rs863224098(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206127973
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs863224098
dbSNP (old)rs863224098
ClinGenrs863224098
ebirs863224098
HLIrs863224098
Exacrs863224098
Gnomadrs863224098
Varsomers863224098
Maprs863224098
PheGenIrs863224098
Biobankrs863224098
1000 genomesrs863224098
hgdprs863224098
ensemblrs863224098
gopubmedrs863224098
geneviewrs863224098
scholarrs863224098
googlers863224098
pharmgkbrs863224098
gwascentralrs863224098
openSNPrs863224098
23andMers863224098
23andMe allrs863224098
SNP Nexus

SNPshotrs863224098
SNPdbers863224098
MSV3drs863224098
GWAS Ctlgrs863224098
Max Magnitude0
ClinVar
Risk rs863224098(A;A)
Alt rs863224098(A;A)
Reference Rs863224098(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.206992697C>T
CLNSRC
CLNACC RCV000199163.1,