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rs139407567

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139407567(C;T)
Make rs139407567(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490807
GeneAIP
is asnp
is mentioned by
dbSNPrs139407567
ebirs139407567
HLIrs139407567
Exacrs139407567
Varsomers139407567
Maprs139407567
PheGenIrs139407567
hapmaprs139407567
1000 genomesrs139407567
hgdprs139407567
ensemblrs139407567
gopubmedrs139407567
geneviewrs139407567
scholarrs139407567
googlers139407567
pharmgkbrs139407567
gwascentralrs139407567
openSNPrs139407567
23andMers139407567
23andMe allrs139407567
SNP Nexus

SNPshotrs139407567
SNPdbers139407567
MSV3drs139407567
GWAS Ctlgrs139407567
Max Magnitude0
ClinVar
Risk rs139407567(T;T)
Alt rs139407567(T;T)
Reference rs139407567(C;C)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258278C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034108.2,