rs200044623
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs200044623(G;G) |
Make rs200044623(G;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 5 |
Position | 35860992 |
Gene | IL7R, LOC105374724 |
is a | snp |
is | mentioned by |
dbSNP | rs200044623 |
dbSNP (classic) | rs200044623 |
ClinGen | rs200044623 |
ebi | rs200044623 |
HLI | rs200044623 |
Exac | rs200044623 |
Gnomad | rs200044623 |
Varsome | rs200044623 |
LitVar | rs200044623 |
Map | rs200044623 |
PheGenI | rs200044623 |
Biobank | rs200044623 |
1000 genomes | rs200044623 |
hgdp | rs200044623 |
ensembl | rs200044623 |
geneview | rs200044623 |
scholar | rs200044623 |
rs200044623 | |
pharmgkb | rs200044623 |
gwascentral | rs200044623 |
openSNP | rs200044623 |
23andMe | rs200044623 |
SNPshot | rs200044623 |
SNPdbe | rs200044623 |
MSV3d | rs200044623 |
GWAS Ctlg | rs200044623 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200044623(G;G) |
Alt | rs200044623(G;G) |
Reference | Rs200044623(T;T) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | IL7R |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.35861094T>G |
CLNSRC | |
CLNACC | RCV000255196.1, |