rs754812742
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 4 | Ichthyosis vulgaris (dry, scaly skin) |
Make rs754812742(A;A) |
Make rs754812742(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 152310981 |
Gene | FLG |
is a | snp |
is | mentioned by |
dbSNP | rs754812742 |
dbSNP (classic) | rs754812742 |
ClinGen | rs754812742 |
ebi | rs754812742 |
HLI | rs754812742 |
Exac | rs754812742 |
Gnomad | rs754812742 |
Varsome | rs754812742 |
LitVar | rs754812742 |
Map | rs754812742 |
PheGenI | rs754812742 |
Biobank | rs754812742 |
1000 genomes | rs754812742 |
hgdp | rs754812742 |
ensembl | rs754812742 |
geneview | rs754812742 |
scholar | rs754812742 |
rs754812742 | |
pharmgkb | rs754812742 |
gwascentral | rs754812742 |
openSNP | rs754812742 |
23andMe | rs754812742 |
SNPshot | rs754812742 |
SNPdbe | rs754812742 |
MSV3d | rs754812742 |
GWAS Ctlg | rs754812742 |
Max Magnitude | 4 |
aka c.3905C>A (p.Ser1302Ter); also c.3905C>T; the former is pathogenic for ichythosis vulgaris
ClinVar | |
---|---|
Risk | rs754812742(A;A) rs754812742(T;T) |
Alt | rs754812742(A;A) rs754812742(T;T) |
Reference | Rs754812742(G;G) |
Significance | Pathogenic |
Disease | Ichthyosis vulgaris |
Variation | info |
Gene | FLG |
CLNDBN | Ichthyosis vulgaris |
Reversed | 0 |
HGVS | NC_000001.10:g.152283457G>T |
CLNSRC | |
CLNACC | RCV000490412.1, |