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rs267606581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606581(C;C)
Make rs267606581(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490829
GeneAIP
is asnp
is mentioned by
dbSNPrs267606581
ebirs267606581
HLIrs267606581
Exacrs267606581
Varsomers267606581
Maprs267606581
PheGenIrs267606581
hapmaprs267606581
1000 genomesrs267606581
hgdprs267606581
ensemblrs267606581
gopubmedrs267606581
geneviewrs267606581
scholarrs267606581
googlers267606581
pharmgkbrs267606581
gwascentralrs267606581
openSNPrs267606581
23andMers267606581
23andMe allrs267606581
SNP Nexus

SNPshotrs267606581
SNPdbers267606581
MSV3drs267606581
GWAS Ctlgrs267606581
Max Magnitude0
ClinVar
Risk rs267606581(C;C)
Alt rs267606581(C;C)
Reference rs267606581(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258300G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034111.2,