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rs140467171

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs140467171(C;C)
Make rs140467171(C;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position57500337
GeneMARS
is asnp
is mentioned by
dbSNPrs140467171
ebirs140467171
HLIrs140467171
Exacrs140467171
Varsomers140467171
Maprs140467171
PheGenIrs140467171
hapmaprs140467171
1000 genomesrs140467171
hgdprs140467171
ensemblrs140467171
gopubmedrs140467171
geneviewrs140467171
scholarrs140467171
googlers140467171
pharmgkbrs140467171
gwascentralrs140467171
openSNPrs140467171
23andMers140467171
23andMe allrs140467171
SNP Nexus

SNPshotrs140467171
SNPdbers140467171
MSV3drs140467171
GWAS Ctlgrs140467171
Max Magnitude0
ClinVar
Risk rs140467171(C;C)
Alt rs140467171(C;C)
Reference rs140467171(T;T)
Significance Pathogenic
Disease Interstitial lung and liver disease
Variation info
Gene MARS
CLNDBN Interstitial lung and liver disease
Reversed 0
HGVS NC_000012.11:g.57894120T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000059332.31,