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rs587777584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777584(A;A)
Make rs587777584(A;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position30921976
GeneVARS2
is asnp
is mentioned by
dbSNPrs587777584
ebirs587777584
HLIrs587777584
Exacrs587777584
Varsomers587777584
Maprs587777584
PheGenIrs587777584
hapmaprs587777584
1000 genomesrs587777584
hgdprs587777584
ensemblrs587777584
gopubmedrs587777584
geneviewrs587777584
scholarrs587777584
googlers587777584
pharmgkbrs587777584
gwascentralrs587777584
openSNPrs587777584
23andMers587777584
23andMe allrs587777584
SNP Nexus

SNPshotrs587777584
SNPdbers587777584
MSV3drs587777584
GWAS Ctlgrs587777584
Max Magnitude0
ClinVar
Risk rs587777584(A;A)
Alt rs587777584(A;A)
Reference rs587777584(C;C)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 20
Variation info
Gene VARS2
CLNDBN Combined oxidative phosphorylation deficiency 20
Reversed 0
HGVS NC_000006.11:g.30889753C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000129935.4,