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rs267606554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606554(A;A)
Make rs267606554(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489456
GeneAIP
is asnp
is mentioned by
dbSNPrs267606554
ebirs267606554
HLIrs267606554
Exacrs267606554
Varsomers267606554
Maprs267606554
PheGenIrs267606554
hapmaprs267606554
1000 genomesrs267606554
hgdprs267606554
ensemblrs267606554
gopubmedrs267606554
geneviewrs267606554
scholarrs267606554
googlers267606554
pharmgkbrs267606554
gwascentralrs267606554
openSNPrs267606554
23andMers267606554
23andMe allrs267606554
SNP Nexus

SNPshotrs267606554
SNPdbers267606554
MSV3drs267606554
GWAS Ctlgrs267606554
Max Magnitude0
ClinVar
Risk rs267606554(A;A)
Alt rs267606554(A;A)
Reference rs267606554(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256927G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034081.2,