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rs267606571

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606571(C;T)
Make rs267606571(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490385
GeneAIP
is asnp
is mentioned by
dbSNPrs267606571
ebirs267606571
HLIrs267606571
Exacrs267606571
Varsomers267606571
Maprs267606571
PheGenIrs267606571
hapmaprs267606571
1000 genomesrs267606571
hgdprs267606571
ensemblrs267606571
gopubmedrs267606571
geneviewrs267606571
scholarrs267606571
googlers267606571
pharmgkbrs267606571
gwascentralrs267606571
openSNPrs267606571
23andMers267606571
23andMe allrs267606571
SNP Nexus

SNPshotrs267606571
SNPdbers267606571
MSV3drs267606571
GWAS Ctlgrs267606571
Max Magnitude0
ClinVar
Risk rs267606571(T;T)
Alt rs267606571(T;T)
Reference rs267606571(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257856C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034098.2,