rs149105551
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs149105551(C;C) |
Make rs149105551(C;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 152309494 |
Gene | FLG |
is a | snp |
is | mentioned by |
dbSNP | rs149105551 |
dbSNP (classic) | rs149105551 |
ClinGen | rs149105551 |
ebi | rs149105551 |
HLI | rs149105551 |
Exac | rs149105551 |
Gnomad | rs149105551 |
Varsome | rs149105551 |
LitVar | rs149105551 |
Map | rs149105551 |
PheGenI | rs149105551 |
Biobank | rs149105551 |
1000 genomes | rs149105551 |
hgdp | rs149105551 |
ensembl | rs149105551 |
geneview | rs149105551 |
scholar | rs149105551 |
rs149105551 | |
pharmgkb | rs149105551 |
gwascentral | rs149105551 |
openSNP | rs149105551 |
23andMe | rs149105551 |
SNPshot | rs149105551 |
SNPdbe | rs149105551 |
MSV3d | rs149105551 |
GWAS Ctlg | rs149105551 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149105551(A;A) rs149105551(C;C) rs149105551(T;T) |
Alt | rs149105551(A;A) rs149105551(C;C) rs149105551(T;T) |
Reference | Rs149105551(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | FLG |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000001.10:g.152281970G>A |
CLNSRC | |
CLNACC | RCV000484307.1, |