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rs267606543

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606543(A;A)
Make rs267606543(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position67487156
GeneAIP
is asnp
is mentioned by
dbSNPrs267606543
ebirs267606543
HLIrs267606543
Exacrs267606543
Varsomers267606543
Maprs267606543
PheGenIrs267606543
hapmaprs267606543
1000 genomesrs267606543
hgdprs267606543
ensemblrs267606543
gopubmedrs267606543
geneviewrs267606543
scholarrs267606543
googlers267606543
pharmgkbrs267606543
gwascentralrs267606543
openSNPrs267606543
23andMers267606543
23andMe allrs267606543
SNP Nexus

SNPshotrs267606543
SNPdbers267606543
MSV3drs267606543
GWAS Ctlgrs267606543
Max Magnitude0
ClinVar
Risk rs267606543(A;A)
Alt rs267606543(A;A)
Reference rs267606543(G;G)
Significance Probable-Pathogenic
Disease Somatotroph adenoma
Variation info
Gene AIP
CLNDBN Somatotroph adenoma
Reversed 0
HGVS NC_000011.9:g.67254627G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000034069.2,