rs267606538

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs267606538(A;A)

Make rs267606538(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67487072

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606538
dbSNP (classic)	rs267606538
ClinGen	rs267606538
ebi	rs267606538
HLI	rs267606538
Exac	rs267606538
Gnomad	rs267606538
Varsome	rs267606538
LitVar	rs267606538
Map	rs267606538
PheGenI	rs267606538
Biobank	rs267606538
1000 genomes	rs267606538
hgdp	rs267606538
ensembl	rs267606538
geneview	rs267606538
scholar	rs267606538
google	rs267606538
pharmgkb	rs267606538
gwascentral	rs267606538
openSNP	rs267606538
23andMe	rs267606538
SNPshot	rs267606538
SNPdbe	rs267606538
MSV3d	rs267606538
GWAS Ctlg	rs267606538

Max Magnitude

0

ClinVar
Risk	rs267606538(A;A) rs267606538(T;T)
Alt	rs267606538(A;A) rs267606538(T;T)
Reference	Rs267606538(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67254543C>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034064.2,