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

rs267606540

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606540(A;A)
Make rs267606540(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67482939
GeneAIP
is asnp
is mentioned by
dbSNPrs267606540
ebirs267606540
HLIrs267606540
Exacrs267606540
Varsomers267606540
Maprs267606540
PheGenIrs267606540
hapmaprs267606540
1000 genomesrs267606540
hgdprs267606540
ensemblrs267606540
gopubmedrs267606540
geneviewrs267606540
scholarrs267606540
googlers267606540
pharmgkbrs267606540
gwascentralrs267606540
openSNPrs267606540
23andMers267606540
23andMe allrs267606540
SNP Nexus

SNPshotrs267606540
SNPdbers267606540
MSV3drs267606540
GWAS Ctlgrs267606540
Max Magnitude0
ClinVar
Risk rs267606540(A;A)
Alt rs267606540(A;A)
Reference rs267606540(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250410G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034117.2,