Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606566(C;T)
Make rs267606566(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490319
GeneAIP
is asnp
is mentioned by
dbSNPrs267606566
ebirs267606566
HLIrs267606566
Exacrs267606566
Varsomers267606566
Maprs267606566
PheGenIrs267606566
hapmaprs267606566
1000 genomesrs267606566
hgdprs267606566
ensemblrs267606566
gopubmedrs267606566
geneviewrs267606566
scholarrs267606566
googlers267606566
pharmgkbrs267606566
gwascentralrs267606566
openSNPrs267606566
23andMers267606566
23andMe allrs267606566
SNP Nexus

SNPshotrs267606566
SNPdbers267606566
MSV3drs267606566
GWAS Ctlgrs267606566
Max Magnitude0
ClinVar
Risk rs267606566(T;T)
Alt rs267606566(T;T)
Reference rs267606566(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257790C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034093.2,