rs752274637
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs752274637(A;A) |
Make rs752274637(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 35737405 |
Gene | CREB3, GBA2 |
is a | snp |
is | mentioned by |
dbSNP | rs752274637 |
dbSNP (classic) | rs752274637 |
ClinGen | rs752274637 |
ebi | rs752274637 |
HLI | rs752274637 |
Exac | rs752274637 |
Gnomad | rs752274637 |
Varsome | rs752274637 |
LitVar | rs752274637 |
Map | rs752274637 |
PheGenI | rs752274637 |
Biobank | rs752274637 |
1000 genomes | rs752274637 |
hgdp | rs752274637 |
ensembl | rs752274637 |
geneview | rs752274637 |
scholar | rs752274637 |
rs752274637 | |
pharmgkb | rs752274637 |
gwascentral | rs752274637 |
openSNP | rs752274637 |
23andMe | rs752274637 |
SNPshot | rs752274637 |
SNPdbe | rs752274637 |
MSV3d | rs752274637 |
GWAS Ctlg | rs752274637 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs752274637(A;A) |
Alt | rs752274637(A;A) |
Reference | Rs752274637(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CREB3 GBA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.35737402G>A |
CLNSRC | |
CLNACC | RCV000171423.1, |