rs138946894
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs138946894(A;A) |
Make rs138946894(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 247423853 |
Gene | NLRP3 |
is a | snp |
is | mentioned by |
dbSNP | rs138946894 |
dbSNP (classic) | rs138946894 |
ClinGen | rs138946894 |
ebi | rs138946894 |
HLI | rs138946894 |
Exac | rs138946894 |
Gnomad | rs138946894 |
Varsome | rs138946894 |
LitVar | rs138946894 |
Map | rs138946894 |
PheGenI | rs138946894 |
Biobank | rs138946894 |
1000 genomes | rs138946894 |
hgdp | rs138946894 |
ensembl | rs138946894 |
geneview | rs138946894 |
scholar | rs138946894 |
rs138946894 | |
pharmgkb | rs138946894 |
gwascentral | rs138946894 |
openSNP | rs138946894 |
23andMe | rs138946894 |
SNPshot | rs138946894 |
SNPdbe | rs138946894 |
MSV3d | rs138946894 |
GWAS Ctlg | rs138946894 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138946894(A;A) rs138946894(C;C) |
Alt | rs138946894(A;A) rs138946894(C;C) |
Reference | Rs138946894(G;G) |
Significance | Pathogenic |
Disease | not specified |
Variation | info |
Gene | NLRP3 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000001.10:g.247587155G>A |
CLNSRC | |
CLNACC | RCV000219739.2, |