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

rs267606588

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CG;CG) 0 common in clinvar
Make rs267606588(AA;AA)
Make rs267606588(AA;CG)
ReferenceGRCh38 38.1/141
Chromosome11
Position67482889
GeneAIP
is asnp
is mentioned by
dbSNPrs267606588
ebirs267606588
HLIrs267606588
Exacrs267606588
Varsomers267606588
Maprs267606588
PheGenIrs267606588
hapmaprs267606588
1000 genomesrs267606588
hgdprs267606588
ensemblrs267606588
gopubmedrs267606588
geneviewrs267606588
scholarrs267606588
googlers267606588
pharmgkbrs267606588
gwascentralrs267606588
openSNPrs267606588
23andMers267606588
23andMe allrs267606588
SNP Nexus

SNPshotrs267606588
SNPdbers267606588
MSV3drs267606588
GWAS Ctlgrs267606588
Max Magnitude0
ClinVar
Risk rs267606588(AA;AA)
Alt rs267606588(AA;AA)
Reference rs267606588(CG;CG)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250360_67250361delCGinsAA
CLNSRC ClinVar GeneReviews
CLNACC RCV000034117.2,