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rs875989831

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs875989831(A;G)
Make rs875989831(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position101565595
GeneTRMT10C
is asnp
is mentioned by
dbSNPrs875989831
ebirs875989831
HLIrs875989831
Exacrs875989831
Varsomers875989831
Maprs875989831
PheGenIrs875989831
hapmaprs875989831
1000 genomesrs875989831
hgdprs875989831
ensemblrs875989831
gopubmedrs875989831
geneviewrs875989831
scholarrs875989831
googlers875989831
pharmgkbrs875989831
gwascentralrs875989831
openSNPrs875989831
23andMers875989831
23andMe allrs875989831
SNP Nexus

SNPshotrs875989831
SNPdbers875989831
MSV3drs875989831
GWAS Ctlgrs875989831
Max Magnitude0
ClinVar
Risk rs875989831(G;G)
Alt rs875989831(G;G)
Reference rs875989831(A;A)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 30
Variation info
Gene TRMT10C
CLNDBN Combined oxidative phosphorylation deficiency 30
Reversed 0
HGVS NC_000003.11:g.101284439A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000225275.1,