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rs121908357

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908357(C;T)
Make rs121908357(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483222
GeneAIP
is asnp
is mentioned by
dbSNPrs121908357
ebirs121908357
HLIrs121908357
Exacrs121908357
Varsomers121908357
Maprs121908357
PheGenIrs121908357
hapmaprs121908357
1000 genomesrs121908357
hgdprs121908357
ensemblrs121908357
gopubmedrs121908357
geneviewrs121908357
scholarrs121908357
googlers121908357
pharmgkbrs121908357
gwascentralrs121908357
openSNPrs121908357
23andMers121908357
23andMe allrs121908357
SNP Nexus

SNPshotrs121908357
SNPdbers121908357
MSV3drs121908357
GWAS Ctlgrs121908357
Max Magnitude0
OMIM605555
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121908357(T;T)
Alt rs121908357(T;T)
Reference rs121908357(C;C)
Significance Other
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250693C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005172.5,