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rs267606546

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606546(C;C)
Make rs267606546(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483160
GeneAIP
is asnp
is mentioned by
dbSNPrs267606546
ebirs267606546
HLIrs267606546
Exacrs267606546
Varsomers267606546
Maprs267606546
PheGenIrs267606546
hapmaprs267606546
1000 genomesrs267606546
hgdprs267606546
ensemblrs267606546
gopubmedrs267606546
geneviewrs267606546
scholarrs267606546
googlers267606546
pharmgkbrs267606546
gwascentralrs267606546
openSNPrs267606546
23andMers267606546
23andMe allrs267606546
SNP Nexus

SNPshotrs267606546
SNPdbers267606546
MSV3drs267606546
GWAS Ctlgrs267606546
Max Magnitude0
ClinVar
Risk rs267606546(C;C)
Alt rs267606546(C;C)
Reference rs267606546(T;T)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250631T>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034072.2,