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rs4727443

From SNPedia

Orientationplus
Stabilizedplus
Make rs4727443(A;A)
Make rs4727443(A;C)
Make rs4727443(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position99995723
is asnp
is mentioned by
dbSNPrs4727443
ebirs4727443
HLIrs4727443
Exacrs4727443
Varsomers4727443
Maprs4727443
PheGenIrs4727443
hapmaprs4727443
1000 genomesrs4727443
hgdprs4727443
ensemblrs4727443
gopubmedrs4727443
geneviewrs4727443
scholarrs4727443
googlers4727443
pharmgkbrs4727443
gwascentralrs4727443
openSNPrs4727443
23andMers4727443
23andMe allrs4727443
SNP Nexus

SNPshotrs4727443
SNPdbers4727443
MSV3drs4727443
GWAS Ctlgrs4727443
GMAF0.4109
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23583980OA-icon.png]
Trait Interstitial lung disease
Title Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.
Risk Allele C
P-val 1E-8
Odds Ratio 1.30 [1.20-1.41]
? (A;A) (A;C) (C;C)