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rs587777433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777433(A;A)
Make rs587777433(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position131180149
GeneLYRM7
is asnp
is mentioned by
dbSNPrs587777433
ebirs587777433
HLIrs587777433
Exacrs587777433
Varsomers587777433
Maprs587777433
PheGenIrs587777433
hapmaprs587777433
1000 genomesrs587777433
hgdprs587777433
ensemblrs587777433
gopubmedrs587777433
geneviewrs587777433
scholarrs587777433
googlers587777433
pharmgkbrs587777433
gwascentralrs587777433
openSNPrs587777433
23andMers587777433
23andMe allrs587777433
SNP Nexus

SNPshotrs587777433
SNPdbers587777433
MSV3drs587777433
GWAS Ctlgrs587777433
Max Magnitude0
ClinVar
Risk rs587777433(A;A)
Alt rs587777433(A;A)
Reference rs587777433(G;G)
Significance Pathogenic
Disease Mitochondrial complex III deficiency
Variation info
Gene LYRM7
CLNDBN Mitochondrial complex III deficiency, nuclear type 8
Reversed 0
HGVS NC_000005.9:g.130515842G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000122742.3,