rs267606589

Orientation

plus

Stabilized

plus

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

Make rs267606589(-;C)

Make rs267606589(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490919

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606589
dbSNP (classic)	rs267606589
ClinGen	rs267606589
ebi	rs267606589
HLI	rs267606589
Exac	rs267606589
Gnomad	rs267606589
Varsome	rs267606589
LitVar	rs267606589
Map	rs267606589
PheGenI	rs267606589
Biobank	rs267606589
1000 genomes	rs267606589
hgdp	rs267606589
ensembl	rs267606589
geneview	rs267606589
scholar	rs267606589
google	rs267606589
pharmgkb	rs267606589
gwascentral	rs267606589
openSNP	rs267606589
23andMe	rs267606589
SNPshot	rs267606589
SNPdbe	rs267606589
MSV3d	rs267606589
GWAS Ctlg	rs267606589

Max Magnitude

0

ClinVar
Risk	rs267606589(C;C)
Alt	rs267606589(C;C)
Reference	Rs267606589(-;-)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258390dupC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034114.2,