rs768061156
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs768061156(G;T) |
Make rs768061156(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 162149170 |
Gene | GABRG2 |
is a | snp |
is | mentioned by |
dbSNP | rs768061156 |
dbSNP (classic) | rs768061156 |
ClinGen | rs768061156 |
ebi | rs768061156 |
HLI | rs768061156 |
Exac | rs768061156 |
Gnomad | rs768061156 |
Varsome | rs768061156 |
LitVar | rs768061156 |
Map | rs768061156 |
PheGenI | rs768061156 |
Biobank | rs768061156 |
1000 genomes | rs768061156 |
hgdp | rs768061156 |
ensembl | rs768061156 |
geneview | rs768061156 |
scholar | rs768061156 |
rs768061156 | |
pharmgkb | rs768061156 |
gwascentral | rs768061156 |
openSNP | rs768061156 |
23andMe | rs768061156 |
SNPshot | rs768061156 |
SNPdbe | rs768061156 |
MSV3d | rs768061156 |
GWAS Ctlg | rs768061156 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs768061156(T;T) |
Alt | rs768061156(T;T) |
Reference | Rs768061156(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | GABRG2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000005.9:g.161576176G>T |
CLNSRC | |
CLNACC | RCV000187532.3, |