rs587778405
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587778405(G;T) |
Make rs587778405(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 35873604 |
Gene | IL7R |
is a | snp |
is | mentioned by |
dbSNP | rs587778405 |
dbSNP (classic) | rs587778405 |
ClinGen | rs587778405 |
ebi | rs587778405 |
HLI | rs587778405 |
Exac | rs587778405 |
Gnomad | rs587778405 |
Varsome | rs587778405 |
LitVar | rs587778405 |
Map | rs587778405 |
PheGenI | rs587778405 |
Biobank | rs587778405 |
1000 genomes | rs587778405 |
hgdp | rs587778405 |
ensembl | rs587778405 |
geneview | rs587778405 |
scholar | rs587778405 |
rs587778405 | |
pharmgkb | rs587778405 |
gwascentral | rs587778405 |
openSNP | rs587778405 |
23andMe | rs587778405 |
SNPshot | rs587778405 |
SNPdbe | rs587778405 |
MSV3d | rs587778405 |
GWAS Ctlg | rs587778405 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587778405(T;T) |
Alt | rs587778405(T;T) |
Reference | Rs587778405(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | IL7R |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.35873706G>T |
CLNSRC | |
CLNACC | RCV000121217.1, RCV000414042.1, |