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rs267606552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606552(C;T)
Make rs267606552(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489411
GeneAIP
is asnp
is mentioned by
dbSNPrs267606552
ebirs267606552
HLIrs267606552
Exacrs267606552
Varsomers267606552
Maprs267606552
PheGenIrs267606552
hapmaprs267606552
1000 genomesrs267606552
hgdprs267606552
ensemblrs267606552
gopubmedrs267606552
geneviewrs267606552
scholarrs267606552
googlers267606552
pharmgkbrs267606552
gwascentralrs267606552
openSNPrs267606552
23andMers267606552
23andMe allrs267606552
SNP Nexus

SNPshotrs267606552
SNPdbers267606552
MSV3drs267606552
GWAS Ctlgrs267606552
Max Magnitude0
ClinVar
Risk rs267606552(T;T)
Alt rs267606552(T;T)
Reference rs267606552(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256882C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034078.2,