rs61736587
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation |
(G;G) | 0 | common in clinvar |
Make rs61736587(A;A) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 7647436 |
Gene | STXBP2 |
is a | snp |
is | mentioned by |
dbSNP | rs61736587 |
dbSNP (classic) | rs61736587 |
ClinGen | rs61736587 |
ebi | rs61736587 |
HLI | rs61736587 |
Exac | rs61736587 |
Gnomad | rs61736587 |
Varsome | rs61736587 |
LitVar | rs61736587 |
Map | rs61736587 |
PheGenI | rs61736587 |
Biobank | rs61736587 |
1000 genomes | rs61736587 |
hgdp | rs61736587 |
ensembl | rs61736587 |
geneview | rs61736587 |
scholar | rs61736587 |
rs61736587 | |
pharmgkb | rs61736587 |
gwascentral | rs61736587 |
openSNP | rs61736587 |
23andMe | rs61736587 |
SNPshot | rs61736587 |
SNPdbe | rs61736587 |
MSV3d | rs61736587 |
GWAS Ctlg | rs61736587 |
Max Magnitude | 3 |
aka c.1621G>A (p.Gly541Ser)
considered pathogenic for familial hemophagocytic lymphohistiocytosis (HLH) in ClinVar
ClinVar | |
---|---|
Risk | rs61736587(A;A) |
Alt | rs61736587(A;A) |
Reference | Rs61736587(G;G) |
Significance | Pathogenic |
Disease | Hemophagocytic lymphohistiocytosis |
Variation | info |
Gene | STXBP2 |
CLNDBN | Hemophagocytic lymphohistiocytosis, familial, 5 |
Reversed | 0 |
HGVS | NC_000019.9:g.7712322G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000024317.2, |