rs876660977
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs876660977(C;C) |
Make rs876660977(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 10673469 |
Gene | JAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs876660977 |
dbSNP (classic) | rs876660977 |
ClinGen | rs876660977 |
ebi | rs876660977 |
HLI | rs876660977 |
Exac | rs876660977 |
Gnomad | rs876660977 |
Varsome | rs876660977 |
LitVar | rs876660977 |
Map | rs876660977 |
PheGenI | rs876660977 |
Biobank | rs876660977 |
1000 genomes | rs876660977 |
hgdp | rs876660977 |
ensembl | rs876660977 |
geneview | rs876660977 |
scholar | rs876660977 |
rs876660977 | |
pharmgkb | rs876660977 |
gwascentral | rs876660977 |
openSNP | rs876660977 |
23andMe | rs876660977 |
SNPshot | rs876660977 |
SNPdbe | rs876660977 |
MSV3d | rs876660977 |
GWAS Ctlg | rs876660977 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660977(C;C) |
Alt | rs876660977(C;C) |
Reference | Rs876660977(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAG1 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000020.10:g.10654117A>G |
CLNSRC | |
CLNACC | RCV000218438.1, |