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rs267606585

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGGACCCAGCC;CTGGACCCAGCC) 0 common in clinvar
Make rs267606585(-;-)
Make rs267606585(-;CTGGACCCAGCC)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490880
GeneAIP
is asnp
is mentioned by
dbSNPrs267606585
ebirs267606585
HLIrs267606585
Exacrs267606585
Varsomers267606585
Maprs267606585
PheGenIrs267606585
hapmaprs267606585
1000 genomesrs267606585
hgdprs267606585
ensemblrs267606585
gopubmedrs267606585
geneviewrs267606585
scholarrs267606585
googlers267606585
pharmgkbrs267606585
gwascentralrs267606585
openSNPrs267606585
23andMers267606585
23andMe allrs267606585
SNP Nexus

SNPshotrs267606585
SNPdbers267606585
MSV3drs267606585
GWAS Ctlgrs267606585
Max Magnitude0
ClinVar
Risk rs267606585(;)
Alt rs267606585(;)
Reference rs267606585(CTGGACCCAGCC;CTGGACCCAGCC)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258351_67258362delCTGGACCCAGCC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034118.2,