rs863223664
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GC;GC) | 0 | common in clinvar |
Make rs863223664(GC;T) |
Make rs863223664(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 10658574 |
Gene | JAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs863223664 |
dbSNP (classic) | rs863223664 |
ClinGen | rs863223664 |
ebi | rs863223664 |
HLI | rs863223664 |
Exac | rs863223664 |
Gnomad | rs863223664 |
Varsome | rs863223664 |
LitVar | rs863223664 |
Map | rs863223664 |
PheGenI | rs863223664 |
Biobank | rs863223664 |
1000 genomes | rs863223664 |
hgdp | rs863223664 |
ensembl | rs863223664 |
geneview | rs863223664 |
scholar | rs863223664 |
rs863223664 | |
pharmgkb | rs863223664 |
gwascentral | rs863223664 |
openSNP | rs863223664 |
23andMe | rs863223664 |
SNPshot | rs863223664 |
SNPdbe | rs863223664 |
MSV3d | rs863223664 |
GWAS Ctlg | rs863223664 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863223664(T;T) |
Alt | rs863223664(T;T) |
Reference | Rs863223664(GC;GC) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAG1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000020.10:g.10639222_10639223delGCinsA |
CLNSRC | |
CLNACC | RCV000198520.1, |