rs199474690
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs199474690(A;T) |
Make rs199474690(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 36575868 |
Gene | RAG1 |
is a | snp |
is | mentioned by |
dbSNP | rs199474690 |
dbSNP (classic) | rs199474690 |
ClinGen | rs199474690 |
ebi | rs199474690 |
HLI | rs199474690 |
Exac | rs199474690 |
Gnomad | rs199474690 |
Varsome | rs199474690 |
LitVar | rs199474690 |
Map | rs199474690 |
PheGenI | rs199474690 |
Biobank | rs199474690 |
1000 genomes | rs199474690 |
hgdp | rs199474690 |
ensembl | rs199474690 |
geneview | rs199474690 |
scholar | rs199474690 |
rs199474690 | |
pharmgkb | rs199474690 |
gwascentral | rs199474690 |
openSNP | rs199474690 |
23andMe | rs199474690 |
SNPshot | rs199474690 |
SNPdbe | rs199474690 |
MSV3d | rs199474690 |
GWAS Ctlg | rs199474690 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs199474690(G;G) rs199474690(T;T) |
Alt | rs199474690(G;G) rs199474690(T;T) |
Reference | Rs199474690(A;A) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RAG1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.36597418A>G; NC_000011.9:g.36597418A>T |
CLNSRC | UniProtKB (protein) UniProtKB (variants) |
CLNACC | RCV000480355.1, RCV000059572.1, |