rs36001797
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs36001797(A;A) |
Make rs36001797(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 36593886 |
Gene | C11orf74, RAG2 |
is a | snp |
is | mentioned by |
dbSNP | rs36001797 |
dbSNP (classic) | rs36001797 |
ClinGen | rs36001797 |
ebi | rs36001797 |
HLI | rs36001797 |
Exac | rs36001797 |
Gnomad | rs36001797 |
Varsome | rs36001797 |
LitVar | rs36001797 |
Map | rs36001797 |
PheGenI | rs36001797 |
Biobank | rs36001797 |
1000 genomes | rs36001797 |
hgdp | rs36001797 |
ensembl | rs36001797 |
geneview | rs36001797 |
scholar | rs36001797 |
rs36001797 | |
pharmgkb | rs36001797 |
gwascentral | rs36001797 |
openSNP | rs36001797 |
23andMe | rs36001797 |
SNPshot | rs36001797 |
SNPdbe | rs36001797 |
MSV3d | rs36001797 |
GWAS Ctlg | rs36001797 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs36001797(A;A) |
Alt | rs36001797(A;A) |
Reference | Rs36001797(G;G) |
Significance | Pathogenic |
Disease | Histiocytic medullary reticulosis |
Variation | info |
Gene | RAG2 C11orf74 |
CLNDBN | Histiocytic medullary reticulosis |
Reversed | 1 |
HGVS | NC_000011.9:g.36615436C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000014014.24, |