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rs1057524865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524865(A;A)
Make rs1057524865(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position5903611
GeneNDUFA11, VMAC
is asnp
is mentioned by
dbSNPrs1057524865
dbSNP (old)rs1057524865
ClinGenrs1057524865
ebirs1057524865
HLIrs1057524865
Exacrs1057524865
Gnomadrs1057524865
Varsomers1057524865
Maprs1057524865
PheGenIrs1057524865
Biobankrs1057524865
1000 genomesrs1057524865
hgdprs1057524865
ensemblrs1057524865
gopubmedrs1057524865
geneviewrs1057524865
scholarrs1057524865
googlers1057524865
pharmgkbrs1057524865
gwascentralrs1057524865
openSNPrs1057524865
23andMers1057524865
23andMe allrs1057524865
SNPshotrs1057524865
SNPdbers1057524865
MSV3drs1057524865
GWAS Ctlgrs1057524865
Max Magnitude0
ClinVar
Risk rs1057524865(A;A)
Alt rs1057524865(A;A)
Reference Rs1057524865(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFA11 VMAC
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.5903622C>T
CLNSRC
CLNACC RCV000428019.1,