rs199885226
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs199885226(G;T) |
Make rs199885226(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 152314107 |
Gene | FLG, FLG-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs199885226 |
dbSNP (classic) | rs199885226 |
ClinGen | rs199885226 |
ebi | rs199885226 |
HLI | rs199885226 |
Exac | rs199885226 |
Gnomad | rs199885226 |
Varsome | rs199885226 |
LitVar | rs199885226 |
Map | rs199885226 |
PheGenI | rs199885226 |
Biobank | rs199885226 |
1000 genomes | rs199885226 |
hgdp | rs199885226 |
ensembl | rs199885226 |
geneview | rs199885226 |
scholar | rs199885226 |
rs199885226 | |
pharmgkb | rs199885226 |
gwascentral | rs199885226 |
openSNP | rs199885226 |
23andMe | rs199885226 |
SNPshot | rs199885226 |
SNPdbe | rs199885226 |
MSV3d | rs199885226 |
GWAS Ctlg | rs199885226 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199885226(C;C) rs199885226(T;T) |
Alt | rs199885226(C;C) rs199885226(T;T) |
Reference | Rs199885226(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG FLG-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152286583G>T |
CLNSRC | |
CLNACC | RCV000358958.1, |