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rs863224103

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224103(A;A)
Make rs863224103(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206127954
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs863224103
ebirs863224103
HLIrs863224103
Exacrs863224103
Varsomers863224103
Maprs863224103
PheGenIrs863224103
hapmaprs863224103
1000 genomesrs863224103
hgdprs863224103
ensemblrs863224103
gopubmedrs863224103
geneviewrs863224103
scholarrs863224103
googlers863224103
pharmgkbrs863224103
gwascentralrs863224103
openSNPrs863224103
23andMers863224103
23andMe allrs863224103
SNP Nexus

SNPshotrs863224103
SNPdbers863224103
MSV3drs863224103
GWAS Ctlgrs863224103
Max Magnitude0
ClinVar
Risk rs863224103(A;A)
Alt rs863224103(A;A)
Reference rs863224103(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.206992678C>T
CLNSRC
CLNACC RCV000198567.2,