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

rs267606548

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606548(A;G)
Make rs267606548(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489295
GeneAIP
is asnp
is mentioned by
dbSNPrs267606548
ebirs267606548
HLIrs267606548
Exacrs267606548
Varsomers267606548
Maprs267606548
PheGenIrs267606548
hapmaprs267606548
1000 genomesrs267606548
hgdprs267606548
ensemblrs267606548
gopubmedrs267606548
geneviewrs267606548
scholarrs267606548
googlers267606548
pharmgkbrs267606548
gwascentralrs267606548
openSNPrs267606548
23andMers267606548
23andMe allrs267606548
SNP Nexus

SNPshotrs267606548
SNPdbers267606548
MSV3drs267606548
GWAS Ctlgrs267606548
Max Magnitude0
ClinVar
Risk rs267606548(G;G)
Alt rs267606548(G;G)
Reference rs267606548(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256766A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034073.2,