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rs267606556

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606556(A;G)
Make rs267606556(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490036
GeneAIP
is asnp
is mentioned by
dbSNPrs267606556
ebirs267606556
HLIrs267606556
Exacrs267606556
Varsomers267606556
Maprs267606556
PheGenIrs267606556
hapmaprs267606556
1000 genomesrs267606556
hgdprs267606556
ensemblrs267606556
gopubmedrs267606556
geneviewrs267606556
scholarrs267606556
googlers267606556
pharmgkbrs267606556
gwascentralrs267606556
openSNPrs267606556
23andMers267606556
23andMe allrs267606556
SNP Nexus

SNPshotrs267606556
SNPdbers267606556
MSV3drs267606556
GWAS Ctlgrs267606556
Max Magnitude0
ClinVar
Risk rs267606556(G;G)
Alt rs267606556(G;G)
Reference rs267606556(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257507A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034082.2,