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rs104894195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894195(C;T)
Make rs104894195(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490910
GeneAIP
is asnp
is mentioned by
dbSNPrs104894195
ebirs104894195
HLIrs104894195
Exacrs104894195
Varsomers104894195
Maprs104894195
PheGenIrs104894195
hapmaprs104894195
1000 genomesrs104894195
hgdprs104894195
ensemblrs104894195
gopubmedrs104894195
geneviewrs104894195
scholarrs104894195
googlers104894195
pharmgkbrs104894195
gwascentralrs104894195
openSNPrs104894195
23andMers104894195
23andMe allrs104894195
SNP Nexus

SNPshotrs104894195
SNPdbers104894195
MSV3drs104894195
GWAS Ctlgrs104894195
Max Magnitude0
OMIM605555
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894195(G,T;G,T)
Alt rs104894195(G,T;G,T)
Reference rs104894195(C;C)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258381C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005166.3,