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

rs267606569

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606569(A;A)
Make rs267606569(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490383
GeneAIP
is asnp
is mentioned by
dbSNPrs267606569
ebirs267606569
HLIrs267606569
Exacrs267606569
Varsomers267606569
Maprs267606569
PheGenIrs267606569
hapmaprs267606569
1000 genomesrs267606569
hgdprs267606569
ensemblrs267606569
gopubmedrs267606569
geneviewrs267606569
scholarrs267606569
googlers267606569
pharmgkbrs267606569
gwascentralrs267606569
openSNPrs267606569
23andMers267606569
23andMe allrs267606569
SNP Nexus

SNPshotrs267606569
SNPdbers267606569
MSV3drs267606569
GWAS Ctlgrs267606569
Max Magnitude0
ClinVar
Risk rs267606569(A;A)
Alt rs267606569(A;A)
Reference rs267606569(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257854G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034096.2,