rs534723946
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs534723946(A;A) |
Make rs534723946(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 132330094 |
Gene | SETX |
is a | snp |
is | mentioned by |
dbSNP | rs534723946 |
dbSNP (classic) | rs534723946 |
ClinGen | rs534723946 |
ebi | rs534723946 |
HLI | rs534723946 |
Exac | rs534723946 |
Gnomad | rs534723946 |
Varsome | rs534723946 |
LitVar | rs534723946 |
Map | rs534723946 |
PheGenI | rs534723946 |
Biobank | rs534723946 |
1000 genomes | rs534723946 |
hgdp | rs534723946 |
ensembl | rs534723946 |
geneview | rs534723946 |
scholar | rs534723946 |
rs534723946 | |
pharmgkb | rs534723946 |
gwascentral | rs534723946 |
openSNP | rs534723946 |
23andMe | rs534723946 |
SNPshot | rs534723946 |
SNPdbe | rs534723946 |
MSV3d | rs534723946 |
GWAS Ctlg | rs534723946 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs534723946(A;A) |
Alt | rs534723946(A;A) |
Reference | Rs534723946(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SETX |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.135205481G>A |
CLNSRC | |
CLNACC | RCV000143813.1, |