rs745516434
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs745516434(C;G) |
Make rs745516434(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 152312459 |
Gene | FLG, FLG-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs745516434 |
dbSNP (classic) | rs745516434 |
ClinGen | rs745516434 |
ebi | rs745516434 |
HLI | rs745516434 |
Exac | rs745516434 |
Gnomad | rs745516434 |
Varsome | rs745516434 |
LitVar | rs745516434 |
Map | rs745516434 |
PheGenI | rs745516434 |
Biobank | rs745516434 |
1000 genomes | rs745516434 |
hgdp | rs745516434 |
ensembl | rs745516434 |
geneview | rs745516434 |
scholar | rs745516434 |
rs745516434 | |
pharmgkb | rs745516434 |
gwascentral | rs745516434 |
openSNP | rs745516434 |
23andMe | rs745516434 |
SNPshot | rs745516434 |
SNPdbe | rs745516434 |
MSV3d | rs745516434 |
GWAS Ctlg | rs745516434 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745516434(G;G) rs745516434(T;T) |
Alt | rs745516434(G;G) rs745516434(T;T) |
Reference | Rs745516434(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG FLG-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152284935C>T |
CLNSRC | |
CLNACC | RCV000335790.1, |