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rs1130426

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1130426(C;T)
Make rs1130426(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position51347036
GeneETFB
is asnp
is mentioned by
dbSNPrs1130426
dbSNP (classic)rs1130426
ClinGenrs1130426
ebirs1130426
HLIrs1130426
Exacrs1130426
Gnomadrs1130426
Varsomers1130426
LitVarrs1130426
Maprs1130426
PheGenIrs1130426
Biobankrs1130426
1000 genomesrs1130426
hgdprs1130426
ensemblrs1130426
geneviewrs1130426
scholarrs1130426
googlers1130426
pharmgkbrs1130426
gwascentralrs1130426
openSNPrs1130426
23andMers1130426
SNPshotrs1130426
SNPdbers1130426
MSV3drs1130426
GWAS Ctlgrs1130426
Merged fromRs3177751
GMAF0.4633
Max Magnitude0
? (C;C) (C;T) (T;T) 28


ClinVar
Risk rs1130426(A;A) rs1130426(G;G) rs1130426(T;T)
Alt rs1130426(A;A) rs1130426(G;G) rs1130426(T;T)
Reference Rs1130426(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene ETFB
CLNDBN not specified
Reversed 1
HGVS NC_000019.9:g.51850290G>A
CLNSRC UniProtKB (protein)
CLNACC RCV000079961.4,