rs267606588

Orientation

plus

Stabilized

plus

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

Make rs267606588(AA;AA)

Make rs267606588(AA;CG)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67482889

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606588
dbSNP (classic)	rs267606588
ClinGen	rs267606588
ebi	rs267606588
HLI	rs267606588
Exac	rs267606588
Gnomad	rs267606588
Varsome	rs267606588
LitVar	rs267606588
Map	rs267606588
PheGenI	rs267606588
Biobank	rs267606588
1000 genomes	rs267606588
hgdp	rs267606588
ensembl	rs267606588
geneview	rs267606588
scholar	rs267606588
google	rs267606588
pharmgkb	rs267606588
gwascentral	rs267606588
openSNP	rs267606588
23andMe	rs267606588
SNPshot	rs267606588
SNPdbe	rs267606588
MSV3d	rs267606588
GWAS Ctlg	rs267606588

Max Magnitude

0

ClinVar
Risk	rs267606588(AA;AA)
Alt	rs267606588(AA;AA)
Reference	Rs267606588(CG;CG)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250360_67250361delCGinsAA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034117.2,