rs375622900
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs375622900(A;A) |
Make rs375622900(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 10641164 |
Gene | JAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs375622900 |
dbSNP (classic) | rs375622900 |
ClinGen | rs375622900 |
ebi | rs375622900 |
HLI | rs375622900 |
Exac | rs375622900 |
Gnomad | rs375622900 |
Varsome | rs375622900 |
LitVar | rs375622900 |
Map | rs375622900 |
PheGenI | rs375622900 |
Biobank | rs375622900 |
1000 genomes | rs375622900 |
hgdp | rs375622900 |
ensembl | rs375622900 |
geneview | rs375622900 |
scholar | rs375622900 |
rs375622900 | |
pharmgkb | rs375622900 |
gwascentral | rs375622900 |
openSNP | rs375622900 |
23andMe | rs375622900 |
SNPshot | rs375622900 |
SNPdbe | rs375622900 |
MSV3d | rs375622900 |
GWAS Ctlg | rs375622900 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs375622900(A;A) |
Alt | rs375622900(A;A) |
Reference | Rs375622900(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | JAG1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.10621812G>C |
CLNSRC | |
CLNACC | RCV000195918.1, |