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rs1805076

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1805076(A;A)
Make rs1805076(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position111764842
GenePPP2R1B
is asnp
is mentioned by
dbSNPrs1805076
ebirs1805076
HLIrs1805076
Exacrs1805076
Varsomers1805076
Maprs1805076
PheGenIrs1805076
hapmaprs1805076
1000 genomesrs1805076
hgdprs1805076
ensemblrs1805076
gopubmedrs1805076
geneviewrs1805076
scholarrs1805076
googlers1805076
pharmgkbrs1805076
gwascentralrs1805076
openSNPrs1805076
23andMers1805076
23andMe allrs1805076
SNP Nexus

SNPshotrs1805076
SNPdbers1805076
MSV3drs1805076
GWAS Ctlgrs1805076
GMAF0.007346
Max Magnitude0
OMIM603113
Desc
Variant0001
Relatedalso
ClinVar
Risk rs1805076(A;A)
Alt rs1805076(A;A)
Reference rs1805076(G;G)
Significance Pathogenic
Disease Lung cancer
Variation info
Gene PPP2R1B
CLNDBN Lung cancer
Reversed 1
HGVS NC_000011.9:g.111635566C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007000.2,


GET Evidence
PPP2R1B-G90D
aa_change Gly90Asp
aa_change_short G90D
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.00799405
summary Associated with increased incidence of cancer.