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rs267606544

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606544(A;A)
Make rs267606544(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67489266
GeneAIP
is asnp
is mentioned by
dbSNPrs267606544
ebirs267606544
HLIrs267606544
Exacrs267606544
Varsomers267606544
Maprs267606544
PheGenIrs267606544
hapmaprs267606544
1000 genomesrs267606544
hgdprs267606544
ensemblrs267606544
gopubmedrs267606544
geneviewrs267606544
scholarrs267606544
googlers267606544
pharmgkbrs267606544
gwascentralrs267606544
openSNPrs267606544
23andMers267606544
23andMe allrs267606544
SNP Nexus

SNPshotrs267606544
SNPdbers267606544
MSV3drs267606544
GWAS Ctlgrs267606544
Max Magnitude0
ClinVar
Risk rs267606544(A;A)
Alt rs267606544(A;A)
Reference rs267606544(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67256737G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034070.2,