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rs267606574

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAC;TAC) 0 common in clinvar
Make rs267606574(-;-)
Make rs267606574(-;TAC)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490412
GeneAIP
is asnp
is mentioned by
dbSNPrs267606574
ebirs267606574
HLIrs267606574
Exacrs267606574
Varsomers267606574
Maprs267606574
PheGenIrs267606574
hapmaprs267606574
1000 genomesrs267606574
hgdprs267606574
ensemblrs267606574
gopubmedrs267606574
geneviewrs267606574
scholarrs267606574
googlers267606574
pharmgkbrs267606574
gwascentralrs267606574
openSNPrs267606574
23andMers267606574
23andMe allrs267606574
SNP Nexus

SNPshotrs267606574
SNPdbers267606574
MSV3drs267606574
GWAS Ctlgrs267606574
Max Magnitude0
ClinVar
Risk rs267606574(;)
Alt rs267606574(;)
Reference rs267606574(TAC;TAC)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257883_67257885delTAC
CLNSRC ClinVar GeneReviews
CLNACC RCV000034101.2,