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rs267606538

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606538(A;A)
Make rs267606538(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487072
GeneAIP
is asnp
is mentioned by
dbSNPrs267606538
ebirs267606538
HLIrs267606538
Exacrs267606538
Varsomers267606538
Maprs267606538
PheGenIrs267606538
hapmaprs267606538
1000 genomesrs267606538
hgdprs267606538
ensemblrs267606538
gopubmedrs267606538
geneviewrs267606538
scholarrs267606538
googlers267606538
pharmgkbrs267606538
gwascentralrs267606538
openSNPrs267606538
23andMers267606538
23andMe allrs267606538
SNP Nexus

SNPshotrs267606538
SNPdbers267606538
MSV3drs267606538
GWAS Ctlgrs267606538
Max Magnitude0
ClinVar
Risk rs267606538(A,T;A,T)
Alt rs267606538(A,T;A,T)
Reference rs267606538(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254543C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034064.2,