rs1341023
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1341023(C;T) |
Make rs1341023(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 20 |
Position | 38304258 |
Gene | BPI |
is a | snp |
is | mentioned by |
dbSNP | rs1341023 |
dbSNP (classic) | rs1341023 |
ClinGen | rs1341023 |
ebi | rs1341023 |
HLI | rs1341023 |
Exac | rs1341023 |
Gnomad | rs1341023 |
Varsome | rs1341023 |
LitVar | rs1341023 |
Map | rs1341023 |
PheGenI | rs1341023 |
Biobank | rs1341023 |
1000 genomes | rs1341023 |
hgdp | rs1341023 |
ensembl | rs1341023 |
geneview | rs1341023 |
scholar | rs1341023 |
rs1341023 | |
pharmgkb | rs1341023 |
gwascentral | rs1341023 |
openSNP | rs1341023 |
23andMe | rs1341023 |
SNPshot | rs1341023 |
SNPdbe | rs1341023 |
MSV3d | rs1341023 |
GWAS Ctlg | rs1341023 |
Max Magnitude | 0 |
[PMID 25000179] 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, |