Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606539

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606539(C;C)
Make rs267606539(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487080
GeneAIP
is asnp
is mentioned by
dbSNPrs267606539
ebirs267606539
HLIrs267606539
Exacrs267606539
Varsomers267606539
Maprs267606539
PheGenIrs267606539
hapmaprs267606539
1000 genomesrs267606539
hgdprs267606539
ensemblrs267606539
gopubmedrs267606539
geneviewrs267606539
scholarrs267606539
googlers267606539
pharmgkbrs267606539
gwascentralrs267606539
openSNPrs267606539
23andMers267606539
23andMe allrs267606539
SNP Nexus

SNPshotrs267606539
SNPdbers267606539
MSV3drs267606539
GWAS Ctlgrs267606539
Max Magnitude0
ClinVar
Risk rs267606539(C,T;C,T)
Alt rs267606539(C,T;C,T)
Reference rs267606539(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254551G>C
CLNSRC ClinVar GeneReviews
CLNACC RCV000034065.2,