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rs587776680

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776680(C;G)
ReferenceGRCh38 38.1/142
Chromosome19
Position18072111
GeneIL12RB1
is asnp
is mentioned by
dbSNPrs587776680
ebirs587776680
HLIrs587776680
Exacrs587776680
Varsomers587776680
Maprs587776680
PheGenIrs587776680
hapmaprs587776680
1000 genomesrs587776680
hgdprs587776680
ensemblrs587776680
gopubmedrs587776680
geneviewrs587776680
scholarrs587776680
googlers587776680
pharmgkbrs587776680
gwascentralrs587776680
openSNPrs587776680
23andMers587776680
23andMe allrs587776680
SNP Nexus

SNPshotrs587776680
SNPdbers587776680
MSV3drs587776680
GWAS Ctlgrs587776680
Max Magnitude0
ClinVar
Risk rs587776680(C;C)
Alt rs587776680(C;C)
Reference rs587776680(G;G)
Significance Pathogenic
Disease Immunodeficiency 30
Variation info
Gene IL12RB1
CLNDBN Immunodeficiency 30
Reversed 1
HGVS NC_000019.9:g.18182921C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008502.3,