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rs267606579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606579(C;T)
Make rs267606579(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490811
GeneAIP
is asnp
is mentioned by
dbSNPrs267606579
ebirs267606579
HLIrs267606579
Exacrs267606579
Varsomers267606579
Maprs267606579
PheGenIrs267606579
hapmaprs267606579
1000 genomesrs267606579
hgdprs267606579
ensemblrs267606579
gopubmedrs267606579
geneviewrs267606579
scholarrs267606579
googlers267606579
pharmgkbrs267606579
gwascentralrs267606579
openSNPrs267606579
23andMers267606579
23andMe allrs267606579
SNP Nexus

SNPshotrs267606579
SNPdbers267606579
MSV3drs267606579
GWAS Ctlgrs267606579
Max Magnitude0
ClinVar
Risk rs267606579(T;T)
Alt rs267606579(T;T)
Reference rs267606579(C;C)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258282C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034109.2,