rs4358188

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs4358188(A;A)

Make rs4358188(A;G)

Reference

GRCh38 38.1/142

Chromosome

20

Position

38318446

Gene

BPI

is a	snp
is	mentioned by
dbSNP	rs4358188
dbSNP (classic)	rs4358188
ClinGen	rs4358188
ebi	rs4358188
HLI	rs4358188
Exac	rs4358188
Gnomad	rs4358188
Varsome	rs4358188
LitVar	rs4358188
Map	rs4358188
PheGenI	rs4358188
Biobank	rs4358188
1000 genomes	rs4358188
hgdp	rs4358188
ensembl	rs4358188
geneview	rs4358188
scholar	rs4358188
google	rs4358188
pharmgkb	rs4358188
gwascentral	rs4358188
openSNP	rs4358188
23andMe	rs4358188
SNPshot	rs4358188
SNPdbe	rs4358188
MSV3d	rs4358188
GWAS Ctlg	rs4358188

Max Magnitude

0

[PMID 25000179] 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,