rs759998394
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs759998394(C;T) |
Make rs759998394(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 151892356 |
Gene | GLRA1 |
is a | snp |
is | mentioned by |
dbSNP | rs759998394 |
dbSNP (classic) | rs759998394 |
ClinGen | rs759998394 |
ebi | rs759998394 |
HLI | rs759998394 |
Exac | rs759998394 |
Gnomad | rs759998394 |
Varsome | rs759998394 |
LitVar | rs759998394 |
Map | rs759998394 |
PheGenI | rs759998394 |
Biobank | rs759998394 |
1000 genomes | rs759998394 |
hgdp | rs759998394 |
ensembl | rs759998394 |
geneview | rs759998394 |
scholar | rs759998394 |
rs759998394 | |
pharmgkb | rs759998394 |
gwascentral | rs759998394 |
openSNP | rs759998394 |
23andMe | rs759998394 |
SNPshot | rs759998394 |
SNPdbe | rs759998394 |
MSV3d | rs759998394 |
GWAS Ctlg | rs759998394 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs759998394(T;T) |
Alt | rs759998394(T;T) |
Reference | Rs759998394(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GLRA1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.151271917C>T |
CLNSRC | |
CLNACC | RCV000493956.1, |