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rs267606560

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606560(C;T)
Make rs267606560(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490119
GeneAIP
is asnp
is mentioned by
dbSNPrs267606560
ebirs267606560
HLIrs267606560
Exacrs267606560
Varsomers267606560
Maprs267606560
PheGenIrs267606560
hapmaprs267606560
1000 genomesrs267606560
hgdprs267606560
ensemblrs267606560
gopubmedrs267606560
geneviewrs267606560
scholarrs267606560
googlers267606560
pharmgkbrs267606560
gwascentralrs267606560
openSNPrs267606560
23andMers267606560
23andMe allrs267606560
SNP Nexus

SNPshotrs267606560
SNPdbers267606560
MSV3drs267606560
GWAS Ctlgrs267606560
Max Magnitude0
ClinVar
Risk rs267606560(A,T;A,T)
Alt rs267606560(A,T;A,T)
Reference rs267606560(C;C)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257590C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034087.2,