rs145119819
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs145119819(A;A) |
Make rs145119819(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 152313060 |
Gene | FLG, FLG-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs145119819 |
dbSNP (classic) | rs145119819 |
ClinGen | rs145119819 |
ebi | rs145119819 |
HLI | rs145119819 |
Exac | rs145119819 |
Gnomad | rs145119819 |
Varsome | rs145119819 |
LitVar | rs145119819 |
Map | rs145119819 |
PheGenI | rs145119819 |
Biobank | rs145119819 |
1000 genomes | rs145119819 |
hgdp | rs145119819 |
ensembl | rs145119819 |
geneview | rs145119819 |
scholar | rs145119819 |
rs145119819 | |
pharmgkb | rs145119819 |
gwascentral | rs145119819 |
openSNP | rs145119819 |
23andMe | rs145119819 |
SNPshot | rs145119819 |
SNPdbe | rs145119819 |
MSV3d | rs145119819 |
GWAS Ctlg | rs145119819 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs145119819(A;A) rs145119819(T;T) |
Alt | rs145119819(A;A) rs145119819(T;T) |
Reference | Rs145119819(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG FLG-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152285536G>T |
CLNSRC | |
CLNACC | RCV000412715.1, |