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

rs104895072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104895072(G;T)
Make rs104895072(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487155
GeneAIP
is asnp
is mentioned by
dbSNPrs104895072
ebirs104895072
HLIrs104895072
Exacrs104895072
Varsomers104895072
Maprs104895072
PheGenIrs104895072
hapmaprs104895072
1000 genomesrs104895072
hgdprs104895072
ensemblrs104895072
gopubmedrs104895072
geneviewrs104895072
scholarrs104895072
googlers104895072
pharmgkbrs104895072
gwascentralrs104895072
openSNPrs104895072
23andMers104895072
23andMe allrs104895072
SNP Nexus

SNPshotrs104895072
SNPdbers104895072
MSV3drs104895072
GWAS Ctlgrs104895072
Max Magnitude0
ClinVar
Risk rs104895072(T;T)
Alt rs104895072(T;T)
Reference rs104895072(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254626G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034068.2,