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rs267606583

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs267606583(AG;GT)
Make rs267606583(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490878
GeneAIP
is asnp
is mentioned by
dbSNPrs267606583
ebirs267606583
HLIrs267606583
Exacrs267606583
Varsomers267606583
Maprs267606583
PheGenIrs267606583
hapmaprs267606583
1000 genomesrs267606583
hgdprs267606583
ensemblrs267606583
gopubmedrs267606583
geneviewrs267606583
scholarrs267606583
googlers267606583
pharmgkbrs267606583
gwascentralrs267606583
openSNPrs267606583
23andMers267606583
23andMe allrs267606583
SNP Nexus

SNPshotrs267606583
SNPdbers267606583
MSV3drs267606583
GWAS Ctlgrs267606583
Max Magnitude0
ClinVar
Risk rs267606583(GT;GT)
Alt rs267606583(GT;GT)
Reference rs267606583(AG;AG)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258349_67258350delAGinsGT
CLNSRC ClinVar GeneReviews
CLNACC RCV000034118.2,