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rs104895073

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104895073(C;T)
Make rs104895073(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490059
GeneAIP
is asnp
is mentioned by
dbSNPrs104895073
ebirs104895073
HLIrs104895073
Exacrs104895073
Varsomers104895073
Maprs104895073
PheGenIrs104895073
hapmaprs104895073
1000 genomesrs104895073
hgdprs104895073
ensemblrs104895073
gopubmedrs104895073
geneviewrs104895073
scholarrs104895073
googlers104895073
pharmgkbrs104895073
gwascentralrs104895073
openSNPrs104895073
23andMers104895073
23andMe allrs104895073
SNP Nexus

SNPshotrs104895073
SNPdbers104895073
MSV3drs104895073
GWAS Ctlgrs104895073
Max Magnitude0
ClinVar
Risk rs104895073(T;T)
Alt rs104895073(T;T)
Reference rs104895073(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257530C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034084.2,