rs201479289
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201479289(A;A) |
Make rs201479289(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 10 |
Position | 49619743 |
Gene | CHAT |
is a | snp |
is | mentioned by |
dbSNP | rs201479289 |
dbSNP (classic) | rs201479289 |
ClinGen | rs201479289 |
ebi | rs201479289 |
HLI | rs201479289 |
Exac | rs201479289 |
Gnomad | rs201479289 |
Varsome | rs201479289 |
LitVar | rs201479289 |
Map | rs201479289 |
PheGenI | rs201479289 |
Biobank | rs201479289 |
1000 genomes | rs201479289 |
hgdp | rs201479289 |
ensembl | rs201479289 |
geneview | rs201479289 |
scholar | rs201479289 |
rs201479289 | |
pharmgkb | rs201479289 |
gwascentral | rs201479289 |
openSNP | rs201479289 |
23andMe | rs201479289 |
SNPshot | rs201479289 |
SNPdbe | rs201479289 |
MSV3d | rs201479289 |
GWAS Ctlg | rs201479289 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201479289(A;A) |
Alt | rs201479289(A;A) |
Reference | Rs201479289(G;G) |
Significance | Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | CHAT |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000010.10:g.50827789G>A |
CLNSRC | |
CLNACC | RCV000260686.1, RCV000331340.1, |