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rs267606580

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267606580(-;-)
Make rs267606580(-;A)
Make rs267606580(A;A)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490824
GeneAIP
is asnp
is mentioned by
dbSNPrs267606580
ebirs267606580
HLIrs267606580
Exacrs267606580
Varsomers267606580
Maprs267606580
PheGenIrs267606580
hapmaprs267606580
1000 genomesrs267606580
hgdprs267606580
ensemblrs267606580
gopubmedrs267606580
geneviewrs267606580
scholarrs267606580
googlers267606580
pharmgkbrs267606580
gwascentralrs267606580
openSNPrs267606580
23andMers267606580
23andMe allrs267606580
SNP Nexus

SNPshotrs267606580
SNPdbers267606580
MSV3drs267606580
GWAS Ctlgrs267606580
Max Magnitude0
ClinVar
Risk rs267606580(A;A)
Alt rs267606580(A;A)
Reference rs267606580(;)
Significance Other
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258295dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005168.6,