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rs1057517914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517914(A;A)
Make rs1057517914(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position5896452
GeneNDUFA11
is asnp
is mentioned by
dbSNPrs1057517914
dbSNP (old)rs1057517914
ClinGenrs1057517914
ebirs1057517914
HLIrs1057517914
Exacrs1057517914
Gnomadrs1057517914
Varsomers1057517914
LitVarrs1057517914
Maprs1057517914
PheGenIrs1057517914
Biobankrs1057517914
1000 genomesrs1057517914
hgdprs1057517914
ensemblrs1057517914
gopubmedrs1057517914
geneviewrs1057517914
scholarrs1057517914
googlers1057517914
pharmgkbrs1057517914
gwascentralrs1057517914
openSNPrs1057517914
23andMers1057517914
23andMe allrs1057517914
SNPshotrs1057517914
SNPdbers1057517914
MSV3drs1057517914
GWAS Ctlgrs1057517914
Max Magnitude0
ClinVar
Risk rs1057517914(A;A)
Alt rs1057517914(A;A)
Reference Rs1057517914(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFA11
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.5896463C>T
CLNSRC
CLNACC RCV000412826.1,