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rs267606577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606577(A;G)
Make rs267606577(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490803
GeneAIP
is asnp
is mentioned by
dbSNPrs267606577
ebirs267606577
HLIrs267606577
Exacrs267606577
Varsomers267606577
Maprs267606577
PheGenIrs267606577
hapmaprs267606577
1000 genomesrs267606577
hgdprs267606577
ensemblrs267606577
gopubmedrs267606577
geneviewrs267606577
scholarrs267606577
googlers267606577
pharmgkbrs267606577
gwascentralrs267606577
openSNPrs267606577
23andMers267606577
23andMe allrs267606577
SNP Nexus

SNPshotrs267606577
SNPdbers267606577
MSV3drs267606577
GWAS Ctlgrs267606577
Max Magnitude0
ClinVar
Risk rs267606577(G;G)
Alt rs267606577(G;G)
Reference rs267606577(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258274A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034105.2,