rs755427292
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs755427292(A;A) |
Make rs755427292(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 10644903 |
Gene | JAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs755427292 |
dbSNP (classic) | rs755427292 |
ClinGen | rs755427292 |
ebi | rs755427292 |
HLI | rs755427292 |
Exac | rs755427292 |
Gnomad | rs755427292 |
Varsome | rs755427292 |
LitVar | rs755427292 |
Map | rs755427292 |
PheGenI | rs755427292 |
Biobank | rs755427292 |
1000 genomes | rs755427292 |
hgdp | rs755427292 |
ensembl | rs755427292 |
geneview | rs755427292 |
scholar | rs755427292 |
rs755427292 | |
pharmgkb | rs755427292 |
gwascentral | rs755427292 |
openSNP | rs755427292 |
23andMe | rs755427292 |
SNPshot | rs755427292 |
SNPdbe | rs755427292 |
MSV3d | rs755427292 |
GWAS Ctlg | rs755427292 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs755427292(A;A) rs755427292(T;T) |
Alt | rs755427292(A;A) rs755427292(T;T) |
Reference | Rs755427292(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAG1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.10625551G>T |
CLNSRC | |
CLNACC | RCV000216570.1, |