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rs1368439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1368439(G;T)
Make rs1368439(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position159315006
GeneIL12B, LOC105377683
is asnp
is mentioned by
dbSNPrs1368439
dbSNP (old)rs1368439
ClinGenrs1368439
ebirs1368439
HLIrs1368439
Exacrs1368439
Gnomadrs1368439
Varsomers1368439
Maprs1368439
PheGenIrs1368439
Biobankrs1368439
1000 genomesrs1368439
hgdprs1368439
ensemblrs1368439
gopubmedrs1368439
geneviewrs1368439
scholarrs1368439
googlers1368439
pharmgkbrs1368439
gwascentralrs1368439
openSNPrs1368439
23andMers1368439
23andMe allrs1368439
SNPshotrs1368439
SNPdbers1368439
MSV3drs1368439
GWAS Ctlgrs1368439
Max Magnitude0
? (G;G) (G;T) (T;T) 28

[PMID 28596683OA-icon.png] Polymorphisms of microRNA target genes IL12B, INSR, CCND1 and IL10 in gastric cancer.


ClinVar
Risk rs1368439(T;T)
Alt rs1368439(T;T)
Reference Rs1368439(G;G)
Significance Non-pathogenic
Disease Familial Atypical Mycobacteriosis
Variation info
Gene IL12B
CLNDBN Familial Atypical Mycobacteriosis, Autosomal Recessive
Reversed 0
HGVS NC_000005.9:g.158742014G>T
CLNSRC
CLNACC RCV000267660.1,