Have questions? Visit https://www.reddit.com/r/SNPedia

rs104895075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs104895075(-;-)
Make rs104895075(-;C)
Make rs104895075(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490332
GeneAIP
is asnp
is mentioned by
dbSNPrs104895075
ebirs104895075
HLIrs104895075
Exacrs104895075
Varsomers104895075
Maprs104895075
PheGenIrs104895075
hapmaprs104895075
1000 genomesrs104895075
hgdprs104895075
ensemblrs104895075
gopubmedrs104895075
geneviewrs104895075
scholarrs104895075
googlers104895075
pharmgkbrs104895075
gwascentralrs104895075
openSNPrs104895075
23andMers104895075
23andMe allrs104895075
SNP Nexus

SNPshotrs104895075
SNPdbers104895075
MSV3drs104895075
GWAS Ctlgrs104895075
Max Magnitude0
ClinVar
Risk rs104895075(C;C)
Alt rs104895075(C;C)
Reference rs104895075(;)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257803dupC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034094.3,