rs761877421
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TC;TC) | 0 | common in clinvar |
Make rs761877421(-;-) |
Make rs761877421(-;TC) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 152313588 |
Gene | FLG, FLG-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs761877421 |
dbSNP (classic) | rs761877421 |
ClinGen | rs761877421 |
ebi | rs761877421 |
HLI | rs761877421 |
Exac | rs761877421 |
Gnomad | rs761877421 |
Varsome | rs761877421 |
LitVar | rs761877421 |
Map | rs761877421 |
PheGenI | rs761877421 |
Biobank | rs761877421 |
1000 genomes | rs761877421 |
hgdp | rs761877421 |
ensembl | rs761877421 |
geneview | rs761877421 |
scholar | rs761877421 |
rs761877421 | |
pharmgkb | rs761877421 |
gwascentral | rs761877421 |
openSNP | rs761877421 |
23andMe | rs761877421 |
SNPshot | rs761877421 |
SNPdbe | rs761877421 |
MSV3d | rs761877421 |
GWAS Ctlg | rs761877421 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs761877421(-;-) |
Alt | rs761877421(-;-) |
Reference | Rs761877421(TC;TC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG FLG-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152286064_152286065delTC |
CLNSRC | |
CLNACC | RCV000490026.1, |