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rs1057524791

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057524791(A;A)
Make rs1057524791(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position18076321
GeneIL12RB1
is asnp
is mentioned by
dbSNPrs1057524791
dbSNP (old)rs1057524791
ClinGenrs1057524791
ebirs1057524791
HLIrs1057524791
Exacrs1057524791
Gnomadrs1057524791
Varsomers1057524791
Maprs1057524791
PheGenIrs1057524791
Biobankrs1057524791
1000 genomesrs1057524791
hgdprs1057524791
ensemblrs1057524791
gopubmedrs1057524791
geneviewrs1057524791
scholarrs1057524791
googlers1057524791
pharmgkbrs1057524791
gwascentralrs1057524791
openSNPrs1057524791
23andMers1057524791
23andMe allrs1057524791
SNPshotrs1057524791
SNPdbers1057524791
MSV3drs1057524791
GWAS Ctlgrs1057524791
Max Magnitude0
ClinVar
Risk rs1057524791(A;A)
Alt rs1057524791(A;A)
Reference Rs1057524791(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IL12RB1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.18187131A>T
CLNSRC
CLNACC RCV000442785.1,