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rs267606547

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606547(-;-)
Make rs267606547(-;C)
Make rs267606547(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483161
GeneAIP
is asnp
is mentioned by
dbSNPrs267606547
ebirs267606547
HLIrs267606547
Exacrs267606547
Varsomers267606547
Maprs267606547
PheGenIrs267606547
hapmaprs267606547
1000 genomesrs267606547
hgdprs267606547
ensemblrs267606547
gopubmedrs267606547
geneviewrs267606547
scholarrs267606547
googlers267606547
pharmgkbrs267606547
gwascentralrs267606547
openSNPrs267606547
23andMers267606547
23andMe allrs267606547
SNP Nexus

SNPshotrs267606547
SNPdbers267606547
MSV3drs267606547
GWAS Ctlgrs267606547
Max Magnitude0
ClinVar
Risk rs267606547(C;C)
Alt rs267606547(C;C)
Reference rs267606547(;)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250632_67250633insC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034076.2,