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rs267606561

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606561(C;C)
Make rs267606561(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490153
GeneAIP
is asnp
is mentioned by
dbSNPrs267606561
ebirs267606561
HLIrs267606561
Exacrs267606561
Varsomers267606561
Maprs267606561
PheGenIrs267606561
hapmaprs267606561
1000 genomesrs267606561
hgdprs267606561
ensemblrs267606561
gopubmedrs267606561
geneviewrs267606561
scholarrs267606561
googlers267606561
pharmgkbrs267606561
gwascentralrs267606561
openSNPrs267606561
23andMers267606561
23andMe allrs267606561
SNP Nexus

SNPshotrs267606561
SNPdbers267606561
MSV3drs267606561
GWAS Ctlgrs267606561
Max Magnitude0
ClinVar
Risk rs267606561(C;C)
Alt rs267606561(C;C)
Reference rs267606561(T;T)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257624T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034088.2,