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rs146407178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs146407178(C;T)
Make rs146407178(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position47582130
GeneNDUFS3
is asnp
is mentioned by
dbSNPrs146407178
dbSNP (classic)rs146407178
ClinGenrs146407178
ebirs146407178
HLIrs146407178
Exacrs146407178
Gnomadrs146407178
Varsomers146407178
LitVarrs146407178
Maprs146407178
PheGenIrs146407178
Biobankrs146407178
1000 genomesrs146407178
hgdprs146407178
ensemblrs146407178
geneviewrs146407178
scholarrs146407178
googlers146407178
pharmgkbrs146407178
gwascentralrs146407178
openSNPrs146407178
23andMers146407178
23andMe allrs146407178
SNPshotrs146407178
SNPdbers146407178
MSV3drs146407178
GWAS Ctlgrs146407178
Max Magnitude0
ClinVar
Risk rs146407178(T;T)
Alt rs146407178(T;T)
Reference Rs146407178(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47603682C>T
CLNSRC
CLNACC RCV000489564.1,