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rs267606568

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606568(G;T)
Make rs267606568(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483228
GeneAIP
is asnp
is mentioned by
dbSNPrs267606568
ebirs267606568
HLIrs267606568
Exacrs267606568
Varsomers267606568
Maprs267606568
PheGenIrs267606568
hapmaprs267606568
1000 genomesrs267606568
hgdprs267606568
ensemblrs267606568
gopubmedrs267606568
geneviewrs267606568
scholarrs267606568
googlers267606568
pharmgkbrs267606568
gwascentralrs267606568
openSNPrs267606568
23andMers267606568
23andMe allrs267606568
SNP Nexus

SNPshotrs267606568
SNPdbers267606568
MSV3drs267606568
GWAS Ctlgrs267606568
Max Magnitude0
ClinVar
Risk rs267606568(T;T)
Alt rs267606568(T;T)
Reference rs267606568(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250699G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034095.2,