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rs267606565

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606565(G;T)
Make rs267606565(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67490316
GeneAIP
is asnp
is mentioned by
dbSNPrs267606565
ebirs267606565
HLIrs267606565
Exacrs267606565
Varsomers267606565
Maprs267606565
PheGenIrs267606565
hapmaprs267606565
1000 genomesrs267606565
hgdprs267606565
ensemblrs267606565
gopubmedrs267606565
geneviewrs267606565
scholarrs267606565
googlers267606565
pharmgkbrs267606565
gwascentralrs267606565
openSNPrs267606565
23andMers267606565
23andMe allrs267606565
SNP Nexus

SNPshotrs267606565
SNPdbers267606565
MSV3drs267606565
GWAS Ctlgrs267606565
Max Magnitude0
ClinVar
Risk rs267606565(T;T)
Alt rs267606565(T;T)
Reference rs267606565(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene MIR6752 AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67257787G>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000034092.2,