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rs199842745

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199842745(A;A)
Make rs199842745(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position5896455
GeneNDUFA11
is asnp
is mentioned by
dbSNPrs199842745
ebirs199842745
HLIrs199842745
Exacrs199842745
Varsomers199842745
Maprs199842745
PheGenIrs199842745
hapmaprs199842745
1000 genomesrs199842745
hgdprs199842745
ensemblrs199842745
gopubmedrs199842745
geneviewrs199842745
scholarrs199842745
googlers199842745
pharmgkbrs199842745
gwascentralrs199842745
openSNPrs199842745
23andMers199842745
23andMe allrs199842745
SNP Nexus

SNPshotrs199842745
SNPdbers199842745
MSV3drs199842745
GWAS Ctlgrs199842745
Max Magnitude0
ClinVar
Risk rs199842745(A,T;A,T)
Alt rs199842745(A,T;A,T)
Reference rs199842745(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFA11
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.5896466C>A
CLNSRC
CLNACC RCV000197389.2,