rs147423300
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs147423300(A;A) |
Make rs147423300(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 35860981 |
Gene | IL7R, LOC105374724 |
is a | snp |
is | mentioned by |
dbSNP | rs147423300 |
dbSNP (classic) | rs147423300 |
ClinGen | rs147423300 |
ebi | rs147423300 |
HLI | rs147423300 |
Exac | rs147423300 |
Gnomad | rs147423300 |
Varsome | rs147423300 |
LitVar | rs147423300 |
Map | rs147423300 |
PheGenI | rs147423300 |
Biobank | rs147423300 |
1000 genomes | rs147423300 |
hgdp | rs147423300 |
ensembl | rs147423300 |
geneview | rs147423300 |
scholar | rs147423300 |
rs147423300 | |
pharmgkb | rs147423300 |
gwascentral | rs147423300 |
openSNP | rs147423300 |
23andMe | rs147423300 |
SNPshot | rs147423300 |
SNPdbe | rs147423300 |
MSV3d | rs147423300 |
GWAS Ctlg | rs147423300 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs147423300(A;A) rs147423300(C;C) |
Alt | rs147423300(A;A) rs147423300(C;C) |
Reference | Rs147423300(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | IL7R |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.35861083T>C |
CLNSRC | |
CLNACC | RCV000483484.1, |