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rs267606582

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGGC;AGGC) 0 common in clinvar
(CAGG;CAGG) 0 common in clinvar
Make rs267606582(-;-)
Make rs267606582(-;AGGC)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490854
GeneAIP
is asnp
is mentioned by
dbSNPrs267606582
ebirs267606582
HLIrs267606582
Exacrs267606582
Varsomers267606582
Maprs267606582
PheGenIrs267606582
hapmaprs267606582
1000 genomesrs267606582
hgdprs267606582
ensemblrs267606582
gopubmedrs267606582
geneviewrs267606582
scholarrs267606582
googlers267606582
pharmgkbrs267606582
gwascentralrs267606582
openSNPrs267606582
23andMers267606582
23andMe allrs267606582
SNP Nexus

SNPshotrs267606582
SNPdbers267606582
MSV3drs267606582
GWAS Ctlgrs267606582
Max Magnitude0
ClinVar
Risk rs267606582(;)
Alt rs267606582(;)
Reference rs267606582(CAGG;CAGG)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258325_67258328delAGGC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034112.2,