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rs863224099

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224099(C;C)
Make rs863224099(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206127881
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs863224099
ebirs863224099
HLIrs863224099
Exacrs863224099
Varsomers863224099
Maprs863224099
PheGenIrs863224099
hapmaprs863224099
1000 genomesrs863224099
hgdprs863224099
ensemblrs863224099
gopubmedrs863224099
geneviewrs863224099
scholarrs863224099
googlers863224099
pharmgkbrs863224099
gwascentralrs863224099
openSNPrs863224099
23andMers863224099
23andMe allrs863224099
SNP Nexus

SNPshotrs863224099
SNPdbers863224099
MSV3drs863224099
GWAS Ctlgrs863224099
Max Magnitude0
ClinVar
Risk rs863224099(C;C)
Alt rs863224099(C;C)
Reference rs863224099(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.206992605C>G
CLNSRC
CLNACC RCV000195727.1,