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rs143592405

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143592405(C;T)
Make rs143592405(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position57512300
GeneMARS, MIR6758
is asnp
is mentioned by
dbSNPrs143592405
ebirs143592405
HLIrs143592405
Exacrs143592405
Varsomers143592405
Maprs143592405
PheGenIrs143592405
hapmaprs143592405
1000 genomesrs143592405
hgdprs143592405
ensemblrs143592405
gopubmedrs143592405
geneviewrs143592405
scholarrs143592405
googlers143592405
pharmgkbrs143592405
gwascentralrs143592405
openSNPrs143592405
23andMers143592405
23andMe allrs143592405
SNP Nexus

SNPshotrs143592405
SNPdbers143592405
MSV3drs143592405
GWAS Ctlgrs143592405
Max Magnitude0
ClinVar
Risk rs143592405(T;T)
Alt rs143592405(T;T)
Reference rs143592405(C;C)
Significance Pathogenic
Disease Pulmonary alveolar proteinosis Interstitial lung and liver disease
Variation info
Gene MARS MIR6758
CLNDBN Pulmonary alveolar proteinosis Interstitial lung and liver disease
Reversed 0
HGVS NC_000012.11:g.57906083C>T
CLNSRC
CLNACC RCV000169765.1, RCV000169767.1, RCV000173000.2,