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rs104894194

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894194(C;T)
Make rs104894194(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483198
GeneAIP
is asnp
is mentioned by
dbSNPrs104894194
ebirs104894194
HLIrs104894194
Exacrs104894194
Varsomers104894194
Maprs104894194
PheGenIrs104894194
hapmaprs104894194
1000 genomesrs104894194
hgdprs104894194
ensemblrs104894194
gopubmedrs104894194
geneviewrs104894194
scholarrs104894194
googlers104894194
pharmgkbrs104894194
gwascentralrs104894194
openSNPrs104894194
23andMers104894194
23andMe allrs104894194
SNP Nexus

SNPshotrs104894194
SNPdbers104894194
MSV3drs104894194
GWAS Ctlgrs104894194
Max Magnitude0
OMIM605555
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894194(T;T)
Alt rs104894194(T;T)
Reference rs104894194(C;C)
Significance Pathogenic
Disease Pituitary adenoma predisposition Prolactinoma Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Pituitary adenoma predisposition Prolactinoma, familial Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250669C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005163.3, RCV000005164.3, RCV000157603.3,