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rs199474823

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199474823(C;C)
Make rs199474823(C;T)
ReferenceGRCh37.p10 37.5/138
ChromosomeMT
Position2991
GeneC1QTNF9B-AS1
is asnp
is mentioned by
dbSNPrs199474823
ebirs199474823
HLIrs199474823
Exacrs199474823
Varsomers199474823
Maprs199474823
PheGenIrs199474823
hapmaprs199474823
1000 genomesrs199474823
hgdprs199474823
ensemblrs199474823
gopubmedrs199474823
geneviewrs199474823
scholarrs199474823
googlers199474823
pharmgkbrs199474823
gwascentralrs199474823
openSNPrs199474823
23andMers199474823
23andMe allrs199474823
SNP Nexus

SNPshotrs199474823
SNPdbers199474823
MSV3drs199474823
GWAS Ctlgrs199474823
Max Magnitude0
ClinVar
Risk rs199474823(C;C)
Alt rs199474823(C;C)
Reference rs199474823(T;T)
Significance Pathogenic
Disease Chloramphenicol resistance
Variation info
Gene
CLNDBN Chloramphenicol resistance
Reversed 0
HGVS NC_012920.1:m.2991T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010252.2,