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rs267606573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267606573(A;G)
Make rs267606573(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490391
GeneAIP
is asnp
is mentioned by
dbSNPrs267606573
ebirs267606573
HLIrs267606573
Exacrs267606573
Varsomers267606573
Maprs267606573
PheGenIrs267606573
hapmaprs267606573
1000 genomesrs267606573
hgdprs267606573
ensemblrs267606573
gopubmedrs267606573
geneviewrs267606573
scholarrs267606573
googlers267606573
pharmgkbrs267606573
gwascentralrs267606573
openSNPrs267606573
23andMers267606573
23andMe allrs267606573
SNP Nexus

SNPshotrs267606573
SNPdbers267606573
MSV3drs267606573
GWAS Ctlgrs267606573
Max Magnitude0
ClinVar
Risk rs267606573(G,T;G,T)
Alt rs267606573(G,T;G,T)
Reference rs267606573(A;A)
Significance Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257862A>G; NC_000011.9:g.67257862A>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034099.2, RCV000034100.2,