Have questions? Visit https://www.reddit.com/r/SNPedia

rs121434495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs121434495(C;C)
Make rs121434495(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18075857
GeneIL12RB1
is asnp
is mentioned by
dbSNPrs121434495
ebirs121434495
HLIrs121434495
Exacrs121434495
Varsomers121434495
Maprs121434495
PheGenIrs121434495
hapmaprs121434495
1000 genomesrs121434495
hgdprs121434495
ensemblrs121434495
gopubmedrs121434495
geneviewrs121434495
scholarrs121434495
googlers121434495
pharmgkbrs121434495
gwascentralrs121434495
openSNPrs121434495
23andMers121434495
23andMe allrs121434495
SNP Nexus

SNPshotrs121434495
SNPdbers121434495
MSV3drs121434495
GWAS Ctlgrs121434495
Max Magnitude0
OMIM601604
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121434495(C;C)
Alt rs121434495(C;C)
Reference rs121434495(T;T)
Significance Pathogenic
Disease Immunodeficiency 30
Variation info
Gene IL12RB1
CLNDBN Immunodeficiency 30
Reversed 1
HGVS NC_000019.9:g.18186667A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008504.3,