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rs267606563

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606563(A;T)
Make rs267606563(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490170
GeneAIP
is asnp
is mentioned by
dbSNPrs267606563
ebirs267606563
HLIrs267606563
Exacrs267606563
Varsomers267606563
Maprs267606563
PheGenIrs267606563
hapmaprs267606563
1000 genomesrs267606563
hgdprs267606563
ensemblrs267606563
gopubmedrs267606563
geneviewrs267606563
scholarrs267606563
googlers267606563
pharmgkbrs267606563
gwascentralrs267606563
openSNPrs267606563
23andMers267606563
23andMe allrs267606563
SNP Nexus

SNPshotrs267606563
SNPdbers267606563
MSV3drs267606563
GWAS Ctlgrs267606563
Max Magnitude0
ClinVar
Risk rs267606563(T;T)
Alt rs267606563(T;T)
Reference rs267606563(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257641A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034090.2,