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rs869025605

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025605(-;-)
Make rs869025605(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position131180113
GeneLYRM7
is asnp
is mentioned by
dbSNPrs869025605
ebirs869025605
HLIrs869025605
Exacrs869025605
Varsomers869025605
Maprs869025605
PheGenIrs869025605
hapmaprs869025605
1000 genomesrs869025605
hgdprs869025605
ensemblrs869025605
gopubmedrs869025605
geneviewrs869025605
scholarrs869025605
googlers869025605
pharmgkbrs869025605
gwascentralrs869025605
openSNPrs869025605
23andMers869025605
23andMe allrs869025605
SNP Nexus

SNPshotrs869025605
SNPdbers869025605
MSV3drs869025605
GWAS Ctlgrs869025605
Max Magnitude0
ClinVar
Risk rs869025605(;)
Alt rs869025605(;)
Reference rs869025605(A;A)
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.130515806delA
CLNSRC OMIM Allelic Variant
CLNACC RCV000208752.1,