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rs11575934

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11575934(A;G)
Make rs11575934(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position18075808
GeneIL12RB1
is asnp
is mentioned by
dbSNPrs11575934
dbSNP (classic)rs11575934
ClinGenrs11575934
ebirs11575934
HLIrs11575934
Exacrs11575934
Gnomadrs11575934
Varsomers11575934
LitVarrs11575934
Maprs11575934
PheGenIrs11575934
Biobankrs11575934
1000 genomesrs11575934
hgdprs11575934
ensemblrs11575934
geneviewrs11575934
scholarrs11575934
googlers11575934
pharmgkbrs11575934
gwascentralrs11575934
openSNPrs11575934
23andMers11575934
SNPshotrs11575934
SNPdbers11575934
MSV3drs11575934
GWAS Ctlgrs11575934
GMAF0.2585
Max Magnitude0

[PMID 23280621OA-icon.png] Nucleotide variation in IL10 and IL12 and their receptors and cervical and vulvar cancer risk: A hybrid case-parent triad and case-control study

? (A;A) (A;G) (G;G)



[PMID 19460324OA-icon.png] A 475 years-old founder effect involving IL12RB1: a highly prevalent mutation conferring Mendelian Susceptibility to Mycobacterial Diseases in European descendants.


[PMID 20350312OA-icon.png] Polymorphisms in genes of interleukin 12 and its receptors and their association with protection against severe malarial anaemia in children in western Kenya.


[PMID 28289589OA-icon.png] Polymorphism of the IL13 gene may be associated with Uterine leiomyomas in Slovenian women.


ClinVar
Risk rs11575934(G;G)
Alt rs11575934(G;G)
Reference Rs11575934(A;A)
Significance Non-pathogenic
Disease Familial Atypical Mycobacteriosis not specified
Variation info
Gene IL12RB1
CLNDBN Familial Atypical Mycobacteriosis, Autosomal Recessive not specified
Reversed 1
HGVS NC_000019.9:g.18186618T>C
CLNSRC
CLNACC RCV000395252.1, RCV000454739.1,