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rs104895074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TCCCGGAC;TCCCGGAC) 0 common in clinvar
Make rs104895074(CCCCGAT;CCCCGAT)
Make rs104895074(CCCCGAT;TCCCGGAC)
ReferenceGRCh38 38.1/141
Chromosome11
Position67483232
GeneAIP
is asnp
is mentioned by
dbSNPrs104895074
ebirs104895074
HLIrs104895074
Exacrs104895074
Varsomers104895074
Maprs104895074
PheGenIrs104895074
hapmaprs104895074
1000 genomesrs104895074
hgdprs104895074
ensemblrs104895074
gopubmedrs104895074
geneviewrs104895074
scholarrs104895074
googlers104895074
pharmgkbrs104895074
gwascentralrs104895074
openSNPrs104895074
23andMers104895074
23andMe allrs104895074
SNP Nexus

SNPshotrs104895074
SNPdbers104895074
MSV3drs104895074
GWAS Ctlgrs104895074
Max Magnitude0
ClinVar
Risk rs104895074(CCCCGAT;CCCCGAT)
Alt rs104895074(CCCCGAT;CCCCGAT)
Reference rs104895074(TCCCGGAC;TCCCGGAC)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67250703_67250710delTCCCGGACinsCCCCGAT
CLNSRC
CLNACC