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rs267606557

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606557(-;-)
Make rs267606557(-;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490069
GeneAIP
is asnp
is mentioned by
dbSNPrs267606557
ebirs267606557
HLIrs267606557
Exacrs267606557
Varsomers267606557
Maprs267606557
PheGenIrs267606557
hapmaprs267606557
1000 genomesrs267606557
hgdprs267606557
ensemblrs267606557
gopubmedrs267606557
geneviewrs267606557
scholarrs267606557
googlers267606557
pharmgkbrs267606557
gwascentralrs267606557
openSNPrs267606557
23andMers267606557
23andMe allrs267606557
SNP Nexus

SNPshotrs267606557
SNPdbers267606557
MSV3drs267606557
GWAS Ctlgrs267606557
Max Magnitude0
ClinVar
Risk rs267606557(;)
Alt rs267606557(;)
Reference rs267606557(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257540delC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034085.2,