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rs267606541

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606541(C;T)
Make rs267606541(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487147
GeneAIP
is asnp
is mentioned by
dbSNPrs267606541
ebirs267606541
HLIrs267606541
Exacrs267606541
Varsomers267606541
Maprs267606541
PheGenIrs267606541
hapmaprs267606541
1000 genomesrs267606541
hgdprs267606541
ensemblrs267606541
gopubmedrs267606541
geneviewrs267606541
scholarrs267606541
googlers267606541
pharmgkbrs267606541
gwascentralrs267606541
openSNPrs267606541
23andMers267606541
23andMe allrs267606541
SNP Nexus

SNPshotrs267606541
SNPdbers267606541
MSV3drs267606541
GWAS Ctlgrs267606541
Max Magnitude0
ClinVar
Risk rs267606541(T;T)
Alt rs267606541(T;T)
Reference rs267606541(C;C)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254618C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034066.2,