rs376589026
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs376589026(G;T) |
Make rs376589026(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 14139302 |
Gene | TMEM43 |
is a | snp |
is | mentioned by |
dbSNP | rs376589026 |
dbSNP (classic) | rs376589026 |
ClinGen | rs376589026 |
ebi | rs376589026 |
HLI | rs376589026 |
Exac | rs376589026 |
Gnomad | rs376589026 |
Varsome | rs376589026 |
LitVar | rs376589026 |
Map | rs376589026 |
PheGenI | rs376589026 |
Biobank | rs376589026 |
1000 genomes | rs376589026 |
hgdp | rs376589026 |
ensembl | rs376589026 |
geneview | rs376589026 |
scholar | rs376589026 |
rs376589026 | |
pharmgkb | rs376589026 |
gwascentral | rs376589026 |
openSNP | rs376589026 |
23andMe | rs376589026 |
SNPshot | rs376589026 |
SNPdbe | rs376589026 |
MSV3d | rs376589026 |
GWAS Ctlg | rs376589026 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs376589026(T;T) |
Alt | rs376589026(T;T) |
Reference | Rs376589026(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | TMEM43 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.14180802G>T |
CLNSRC | |
CLNACC | RCV000039374.2, |