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rs397515421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515421(A;A)
Make rs397515421(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position151405787
GeneRMND1
is asnp
is mentioned by
dbSNPrs397515421
ebirs397515421
HLIrs397515421
Exacrs397515421
Varsomers397515421
Maprs397515421
PheGenIrs397515421
hapmaprs397515421
1000 genomesrs397515421
hgdprs397515421
ensemblrs397515421
gopubmedrs397515421
geneviewrs397515421
scholarrs397515421
googlers397515421
pharmgkbrs397515421
gwascentralrs397515421
openSNPrs397515421
23andMers397515421
23andMe allrs397515421
SNP Nexus

SNPshotrs397515421
SNPdbers397515421
MSV3drs397515421
GWAS Ctlgrs397515421
Max Magnitude0
ClinVar
Risk rs397515421(A;A)
Alt rs397515421(A;A)
Reference rs397515421(G;G)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 11
Variation info
Gene RMND1
CLNDBN Combined oxidative phosphorylation deficiency 11
Reversed 1
HGVS NC_000006.11:g.151726922C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032984.2,