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rs267606589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606589(-;-)
Make rs267606589(-;C)
Make rs267606589(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490919
GeneAIP
is asnp
is mentioned by
dbSNPrs267606589
ebirs267606589
HLIrs267606589
Exacrs267606589
Varsomers267606589
Maprs267606589
PheGenIrs267606589
hapmaprs267606589
1000 genomesrs267606589
hgdprs267606589
ensemblrs267606589
gopubmedrs267606589
geneviewrs267606589
scholarrs267606589
googlers267606589
pharmgkbrs267606589
gwascentralrs267606589
openSNPrs267606589
23andMers267606589
23andMe allrs267606589
SNP Nexus

SNPshotrs267606589
SNPdbers267606589
MSV3drs267606589
GWAS Ctlgrs267606589
Max Magnitude0
ClinVar
Risk rs267606589(C;C)
Alt rs267606589(C;C)
Reference rs267606589(;)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258390dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034114.2,