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rs267606549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606549(-;-)
Make rs267606549(-;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489337
GeneAIP
is asnp
is mentioned by
dbSNPrs267606549
ebirs267606549
HLIrs267606549
Exacrs267606549
Varsomers267606549
Maprs267606549
PheGenIrs267606549
hapmaprs267606549
1000 genomesrs267606549
hgdprs267606549
ensemblrs267606549
gopubmedrs267606549
geneviewrs267606549
scholarrs267606549
googlers267606549
pharmgkbrs267606549
gwascentralrs267606549
openSNPrs267606549
23andMers267606549
23andMe allrs267606549
SNP Nexus

SNPshotrs267606549
SNPdbers267606549
MSV3drs267606549
GWAS Ctlgrs267606549
Max Magnitude0
ClinVar
Risk rs267606549(;)
Alt rs267606549(;)
Reference rs267606549(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256808delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000034074.2,