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rs1341023

From SNPedia

Orientationplus
Stabilizedplus
Make rs1341023(C;C)
Make rs1341023(C;T)
Make rs1341023(T;T)
ReferenceGRCh38 38.1/142
Chromosome20
Position38304258
GeneBPI
is asnp
is mentioned by
dbSNPrs1341023
ClinGenrs1341023
ebirs1341023
HLIrs1341023
Exacrs1341023
Varsomers1341023
Maprs1341023
PheGenIrs1341023
hapmaprs1341023
1000 genomesrs1341023
hgdprs1341023
ensemblrs1341023
gopubmedrs1341023
geneviewrs1341023
scholarrs1341023
googlers1341023
pharmgkbrs1341023
gwascentralrs1341023
openSNPrs1341023
23andMers1341023
23andMe allrs1341023
SNP Nexus

SNPshotrs1341023
SNPdbers1341023
MSV3drs1341023
GWAS Ctlgrs1341023
Max Magnitude

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


ClinVar
Risk rs1341023(T;T)
Alt rs1341023(T;T)
Reference rs1341023(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene BPI
CLNDBN not specified
Reversed 0
HGVS NC_000020.10:g.36932660C>T
CLNSRC
CLNACC RCV000455313.1,