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rs267606551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606551(-;-)
Make rs267606551(-;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489391
GeneAIP
is asnp
is mentioned by
dbSNPrs267606551
ClinGenrs267606551
ebirs267606551
HLIrs267606551
Exacrs267606551
Varsomers267606551
Maprs267606551
PheGenIrs267606551
hapmaprs267606551
1000 genomesrs267606551
hgdprs267606551
ensemblrs267606551
gopubmedrs267606551
geneviewrs267606551
scholarrs267606551
googlers267606551
pharmgkbrs267606551
gwascentralrs267606551
openSNPrs267606551
23andMers267606551
23andMe allrs267606551
SNP Nexus

SNPshotrs267606551
SNPdbers267606551
MSV3drs267606551
GWAS Ctlgrs267606551
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs267606551(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256862delA
CLNSRC ClinVar GeneReviews
CLNACC RCV000034077.2,