rs200275281
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs200275281(C;G) |
Make rs200275281(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 19 |
Position | 39504079 |
Gene | DLL3 |
is a | snp |
is | mentioned by |
dbSNP | rs200275281 |
dbSNP (classic) | rs200275281 |
ClinGen | rs200275281 |
ebi | rs200275281 |
HLI | rs200275281 |
Exac | rs200275281 |
Gnomad | rs200275281 |
Varsome | rs200275281 |
LitVar | rs200275281 |
Map | rs200275281 |
PheGenI | rs200275281 |
Biobank | rs200275281 |
1000 genomes | rs200275281 |
hgdp | rs200275281 |
ensembl | rs200275281 |
geneview | rs200275281 |
scholar | rs200275281 |
rs200275281 | |
pharmgkb | rs200275281 |
gwascentral | rs200275281 |
openSNP | rs200275281 |
23andMe | rs200275281 |
SNPshot | rs200275281 |
SNPdbe | rs200275281 |
MSV3d | rs200275281 |
GWAS Ctlg | rs200275281 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200275281(G;G) rs200275281(T;T) |
Alt | rs200275281(G;G) rs200275281(T;T) |
Reference | Rs200275281(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | DLL3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.39994719C>T |
CLNSRC | |
CLNACC | RCV000426077.1, |