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rs587779413

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779413(A;A)
Make rs587779413(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position68050224
GeneTCIRG1
is asnp
is mentioned by
dbSNPrs587779413
ebirs587779413
HLIrs587779413
Exacrs587779413
Varsomers587779413
Maprs587779413
PheGenIrs587779413
hapmaprs587779413
1000 genomesrs587779413
hgdprs587779413
ensemblrs587779413
gopubmedrs587779413
geneviewrs587779413
scholarrs587779413
googlers587779413
pharmgkbrs587779413
gwascentralrs587779413
openSNPrs587779413
23andMers587779413
23andMe allrs587779413
SNP Nexus

SNPshotrs587779413
SNPdbers587779413
MSV3drs587779413
GWAS Ctlgrs587779413
Max Magnitude0
ClinVar
Risk rs587779413(A;A)
Alt rs587779413(A;A)
Reference rs587779413(C;C)
Significance Pathogenic
Disease congenital neutropenia Severe congenital neutropenia autosomal dominant
Variation info
Gene TCIRG1
CLNDBN congenital neutropenia Severe congenital neutropenia autosomal dominant
Reversed 0
HGVS NC_000011.9:g.67817691C>A
CLNSRC
CLNACC RCV000133575.1, RCV000224333.1,