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rs267606542

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GAAGG;GAAGG) 0 common in clinvar
Make rs267606542(-;-)
Make rs267606542(-;GAAGG)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487150
GeneAIP
is asnp
is mentioned by
dbSNPrs267606542
ebirs267606542
HLIrs267606542
Exacrs267606542
Varsomers267606542
Maprs267606542
PheGenIrs267606542
hapmaprs267606542
1000 genomesrs267606542
hgdprs267606542
ensemblrs267606542
gopubmedrs267606542
geneviewrs267606542
scholarrs267606542
googlers267606542
pharmgkbrs267606542
gwascentralrs267606542
openSNPrs267606542
23andMers267606542
23andMe allrs267606542
SNP Nexus

SNPshotrs267606542
SNPdbers267606542
MSV3drs267606542
GWAS Ctlgrs267606542
Max Magnitude0
ClinVar
Risk rs267606542(;)
Alt rs267606542(;)
Reference rs267606542(GAAGG;GAAGG)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254621_67254625delGAAGG
CLNSRC ClinVar GeneReviews
CLNACC RCV000034067.2,