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rs199474824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199474824(A;A)
Make rs199474824(A;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeMT
Position2939
is asnp
is mentioned by
dbSNPrs199474824
dbSNP (classic)rs199474824
ClinGenrs199474824
ebirs199474824
HLIrs199474824
Exacrs199474824
Gnomadrs199474824
Varsomers199474824
LitVarrs199474824
Maprs199474824
PheGenIrs199474824
Biobankrs199474824
1000 genomesrs199474824
hgdprs199474824
ensemblrs199474824
geneviewrs199474824
scholarrs199474824
googlers199474824
pharmgkbrs199474824
gwascentralrs199474824
openSNPrs199474824
23andMers199474824
SNPshotrs199474824
SNPdbers199474824
MSV3drs199474824
GWAS Ctlgrs199474824
Max Magnitude0
ClinVar
Risk rs199474824(A;A)
Alt rs199474824(A;A)
Reference Rs199474824(C;C)
Significance Pathogenic
Disease Chloramphenicol resistance
Variation info
Gene
CLNDBN Chloramphenicol resistance
Reversed 0
HGVS NC_012920.1:m.2939C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010253.4,