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rs61736587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61736587(A;A)
Make rs61736587(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position7647436
GeneSTXBP2
is asnp
is mentioned by
dbSNPrs61736587
ebirs61736587
HLIrs61736587
Exacrs61736587
Varsomers61736587
Maprs61736587
PheGenIrs61736587
hapmaprs61736587
1000 genomesrs61736587
hgdprs61736587
ensemblrs61736587
gopubmedrs61736587
geneviewrs61736587
scholarrs61736587
googlers61736587
pharmgkbrs61736587
gwascentralrs61736587
openSNPrs61736587
23andMers61736587
23andMe allrs61736587
SNP Nexus

SNPshotrs61736587
SNPdbers61736587
MSV3drs61736587
GWAS Ctlgrs61736587
Max Magnitude0
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,