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rs4358188

From SNPedia

Orientationplus
Stabilizedplus
Make rs4358188(A;A)
Make rs4358188(A;G)
Make rs4358188(G;G)
ReferenceGRCh38 38.1/142
Chromosome20
Position38318446
GeneBPI
is asnp
is mentioned by
dbSNPrs4358188
ClinGenrs4358188
ebirs4358188
HLIrs4358188
Exacrs4358188
Varsomers4358188
Maprs4358188
PheGenIrs4358188
hapmaprs4358188
1000 genomesrs4358188
hgdprs4358188
ensemblrs4358188
gopubmedrs4358188
geneviewrs4358188
scholarrs4358188
googlers4358188
pharmgkbrs4358188
gwascentralrs4358188
openSNPrs4358188
23andMers4358188
23andMe allrs4358188
SNP Nexus

SNPshotrs4358188
SNPdbers4358188
MSV3drs4358188
GWAS Ctlgrs4358188
Max Magnitude

[PMID 25000179OA-icon.png] Genetic polymorphisms and sepsis in premature neonates


ClinVar
Risk rs4358188(A;A)
Alt rs4358188(A;A)
Reference rs4358188(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene BPI
CLNDBN not specified
Reversed 0
HGVS NC_000020.10:g.36946848G>A
CLNSRC
CLNACC RCV000456105.1,