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rs587776807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776807(-;-)
Make rs587776807(-;T)
Make rs587776807(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position159323098
GeneIL12B
is asnp
is mentioned by
dbSNPrs587776807
ebirs587776807
HLIrs587776807
Exacrs587776807
Varsomers587776807
Maprs587776807
PheGenIrs587776807
hapmaprs587776807
1000 genomesrs587776807
hgdprs587776807
ensemblrs587776807
gopubmedrs587776807
geneviewrs587776807
scholarrs587776807
googlers587776807
pharmgkbrs587776807
gwascentralrs587776807
openSNPrs587776807
23andMers587776807
23andMe allrs587776807
SNP Nexus

SNPshotrs587776807
SNPdbers587776807
MSV3drs587776807
GWAS Ctlgrs587776807
Max Magnitude0
ClinVar
Risk rs587776807(T;T)
Alt rs587776807(T;T)
Reference rs587776807(;)
Significance Pathogenic
Disease Immunodeficiency 29
Variation info
Gene IL12B
CLNDBN Immunodeficiency 29
Reversed 0
HGVS NC_000005.9:g.158750106dupT
CLNSRC OMIM Allelic Variant
CLNACC RCV000015098.27,