rs876661066
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876661066(A;A) |
Make rs876661066(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 10673449 |
Gene | JAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs876661066 |
dbSNP (classic) | rs876661066 |
ClinGen | rs876661066 |
ebi | rs876661066 |
HLI | rs876661066 |
Exac | rs876661066 |
Gnomad | rs876661066 |
Varsome | rs876661066 |
LitVar | rs876661066 |
Map | rs876661066 |
PheGenI | rs876661066 |
Biobank | rs876661066 |
1000 genomes | rs876661066 |
hgdp | rs876661066 |
ensembl | rs876661066 |
geneview | rs876661066 |
scholar | rs876661066 |
rs876661066 | |
pharmgkb | rs876661066 |
gwascentral | rs876661066 |
openSNP | rs876661066 |
23andMe | rs876661066 |
SNPshot | rs876661066 |
SNPdbe | rs876661066 |
MSV3d | rs876661066 |
GWAS Ctlg | rs876661066 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876661066(A;A) |
Alt | rs876661066(A;A) |
Reference | Rs876661066(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAG1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000020.10:g.10654097C>T |
CLNSRC | |
CLNACC | RCV000221204.1, |