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rs121908356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908356(A;A)
Make rs121908356(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490804
GeneAIP, MIR6752
is asnp
is mentioned by
dbSNPrs121908356
ebirs121908356
HLIrs121908356
Exacrs121908356
Varsomers121908356
Maprs121908356
PheGenIrs121908356
hapmaprs121908356
1000 genomesrs121908356
hgdprs121908356
ensemblrs121908356
gopubmedrs121908356
geneviewrs121908356
scholarrs121908356
googlers121908356
pharmgkbrs121908356
gwascentralrs121908356
openSNPrs121908356
23andMers121908356
23andMe allrs121908356
SNP Nexus

SNPshotrs121908356
SNPdbers121908356
MSV3drs121908356
GWAS Ctlgrs121908356
Max Magnitude0
OMIM605555
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908356(A;A)
Alt rs121908356(A;A)
Reference rs121908356(C;C)
Significance Pathogenic
Disease Pituitary adenoma predisposition Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Pituitary adenoma predisposition Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67258275C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005170.3, RCV000034106.2,