rs544389920
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs544389920(C;T) |
Make rs544389920(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 158658952 |
Gene | GFM1 |
is a | snp |
is | mentioned by |
dbSNP | rs544389920 |
dbSNP (classic) | rs544389920 |
ClinGen | rs544389920 |
ebi | rs544389920 |
HLI | rs544389920 |
Exac | rs544389920 |
Gnomad | rs544389920 |
Varsome | rs544389920 |
LitVar | rs544389920 |
Map | rs544389920 |
PheGenI | rs544389920 |
Biobank | rs544389920 |
1000 genomes | rs544389920 |
hgdp | rs544389920 |
ensembl | rs544389920 |
geneview | rs544389920 |
scholar | rs544389920 |
rs544389920 | |
pharmgkb | rs544389920 |
gwascentral | rs544389920 |
openSNP | rs544389920 |
23andMe | rs544389920 |
SNPshot | rs544389920 |
SNPdbe | rs544389920 |
MSV3d | rs544389920 |
GWAS Ctlg | rs544389920 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs544389920(T;T) |
Alt | rs544389920(T;T) |
Reference | Rs544389920(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GFM1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000003.11:g.158376741C>T |
CLNSRC | |
CLNACC | RCV000197604.1, |