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rs267606575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606575(A;G)
Make rs267606575(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490439
GeneAIP
is asnp
is mentioned by
dbSNPrs267606575
ebirs267606575
HLIrs267606575
Exacrs267606575
Varsomers267606575
Maprs267606575
PheGenIrs267606575
hapmaprs267606575
1000 genomesrs267606575
hgdprs267606575
ensemblrs267606575
gopubmedrs267606575
geneviewrs267606575
scholarrs267606575
googlers267606575
pharmgkbrs267606575
gwascentralrs267606575
openSNPrs267606575
23andMers267606575
23andMe allrs267606575
SNP Nexus

SNPshotrs267606575
SNPdbers267606575
MSV3drs267606575
GWAS Ctlgrs267606575
Max Magnitude0
ClinVar
Risk rs267606575(G;G)
Alt rs267606575(G;G)
Reference rs267606575(A;A)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257910A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000034103.2,