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rs200387097

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200387097(C;T)
Make rs200387097(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position240014786
GeneNDUFA10
is asnp
is mentioned by
dbSNPrs200387097
ebirs200387097
HLIrs200387097
Exacrs200387097
Varsomers200387097
Maprs200387097
PheGenIrs200387097
hapmaprs200387097
1000 genomesrs200387097
hgdprs200387097
ensemblrs200387097
gopubmedrs200387097
geneviewrs200387097
scholarrs200387097
googlers200387097
pharmgkbrs200387097
gwascentralrs200387097
openSNPrs200387097
23andMers200387097
23andMe allrs200387097
SNP Nexus

SNPshotrs200387097
SNPdbers200387097
MSV3drs200387097
GWAS Ctlgrs200387097
Max Magnitude0
ClinVar
Risk rs200387097(G,T;G,T)
Alt rs200387097(G,T;G,T)
Reference rs200387097(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFA10
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.240954203C>G
CLNSRC
CLNACC RCV000198629.1,