rs777181377
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs777181377(A;A) |
Make rs777181377(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 1 |
Position | 152312668 |
Gene | FLG, FLG-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs777181377 |
dbSNP (classic) | rs777181377 |
ClinGen | rs777181377 |
ebi | rs777181377 |
HLI | rs777181377 |
Exac | rs777181377 |
Gnomad | rs777181377 |
Varsome | rs777181377 |
LitVar | rs777181377 |
Map | rs777181377 |
PheGenI | rs777181377 |
Biobank | rs777181377 |
1000 genomes | rs777181377 |
hgdp | rs777181377 |
ensembl | rs777181377 |
geneview | rs777181377 |
scholar | rs777181377 |
rs777181377 | |
pharmgkb | rs777181377 |
gwascentral | rs777181377 |
openSNP | rs777181377 |
23andMe | rs777181377 |
SNPshot | rs777181377 |
SNPdbe | rs777181377 |
MSV3d | rs777181377 |
GWAS Ctlg | rs777181377 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs777181377(A;A) |
Alt | rs777181377(A;A) |
Reference | Rs777181377(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG FLG-AS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152285144G>A |
CLNSRC | |
CLNACC | RCV000293346.1, |