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rs267606545

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Make rs267606545(-;-)
Make rs267606545(-;GT)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489273
GeneAIP
is asnp
is mentioned by
dbSNPrs267606545
ebirs267606545
HLIrs267606545
Exacrs267606545
Varsomers267606545
Maprs267606545
PheGenIrs267606545
hapmaprs267606545
1000 genomesrs267606545
hgdprs267606545
ensemblrs267606545
gopubmedrs267606545
geneviewrs267606545
scholarrs267606545
googlers267606545
pharmgkbrs267606545
gwascentralrs267606545
openSNPrs267606545
23andMers267606545
23andMe allrs267606545
SNP Nexus

SNPshotrs267606545
SNPdbers267606545
MSV3drs267606545
GWAS Ctlgrs267606545
Max Magnitude0
ClinVar
Risk rs267606545(;)
Alt rs267606545(;)
Reference rs267606545(GT;GT)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256744_67256745delGT
CLNSRC ClinVar GeneReviews
CLNACC RCV000034071.2,