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rs202006716

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs202006716(A;A)
Make rs202006716(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490160
GeneAIP
is asnp
is mentioned by
dbSNPrs202006716
ebirs202006716
HLIrs202006716
Exacrs202006716
Varsomers202006716
Maprs202006716
PheGenIrs202006716
hapmaprs202006716
1000 genomesrs202006716
hgdprs202006716
ensemblrs202006716
gopubmedrs202006716
geneviewrs202006716
scholarrs202006716
googlers202006716
pharmgkbrs202006716
gwascentralrs202006716
openSNPrs202006716
23andMers202006716
23andMe allrs202006716
SNP Nexus

SNPshotrs202006716
SNPdbers202006716
MSV3drs202006716
GWAS Ctlgrs202006716
Max Magnitude0
ClinVar
Risk rs202006716(A;A)
Alt rs202006716(A;A)
Reference rs202006716(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257631G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034089.2,