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rs863224097

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224097(A;T)
Make rs863224097(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206130100
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs863224097
ebirs863224097
HLIrs863224097
Exacrs863224097
Varsomers863224097
Maprs863224097
PheGenIrs863224097
hapmaprs863224097
1000 genomesrs863224097
hgdprs863224097
ensemblrs863224097
gopubmedrs863224097
geneviewrs863224097
scholarrs863224097
googlers863224097
pharmgkbrs863224097
gwascentralrs863224097
openSNPrs863224097
23andMers863224097
23andMe allrs863224097
SNP Nexus

SNPshotrs863224097
SNPdbers863224097
MSV3drs863224097
GWAS Ctlgrs863224097
Max Magnitude0
ClinVar
Risk rs863224097(T;T)
Alt rs863224097(T;T)
Reference rs863224097(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.206994824T>A
CLNSRC
CLNACC RCV000197278.2,