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rs115079861

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs115079861(C;T)
Make rs115079861(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position151405236
GeneRMND1
is asnp
is mentioned by
dbSNPrs115079861
ebirs115079861
HLIrs115079861
Exacrs115079861
Varsomers115079861
Maprs115079861
PheGenIrs115079861
hapmaprs115079861
1000 genomesrs115079861
hgdprs115079861
ensemblrs115079861
gopubmedrs115079861
geneviewrs115079861
scholarrs115079861
googlers115079861
pharmgkbrs115079861
gwascentralrs115079861
openSNPrs115079861
23andMers115079861
23andMe allrs115079861
SNP Nexus

SNPshotrs115079861
SNPdbers115079861
MSV3drs115079861
GWAS Ctlgrs115079861
Max Magnitude0
ClinVar
Risk rs115079861(G,T;G,T)
Alt rs115079861(G,T;G,T)
Reference rs115079861(C;C)
Significance Pathogenic
Disease Combined oxidative phosphorylation deficiency 11 not specified
Variation info
Gene RMND1
CLNDBN Combined oxidative phosphorylation deficiency 11 not specified
Reversed 0
HGVS NC_000006.11:g.151726371C>G; NC_000006.11:g.151726371C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000132559.2, RCV000127785.1,