rs267606582

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGGC;AGGC)	0	common in clinvar
(CAGG;CAGG)	0	common in clinvar

Make rs267606582(-;-)

Make rs267606582(-;AGGC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490854

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606582
dbSNP (classic)	rs267606582
ClinGen	rs267606582
ebi	rs267606582
HLI	rs267606582
Exac	rs267606582
Gnomad	rs267606582
Varsome	rs267606582
LitVar	rs267606582
Map	rs267606582
PheGenI	rs267606582
Biobank	rs267606582
1000 genomes	rs267606582
hgdp	rs267606582
ensembl	rs267606582
geneview	rs267606582
scholar	rs267606582
google	rs267606582
pharmgkb	rs267606582
gwascentral	rs267606582
openSNP	rs267606582
23andMe	rs267606582
SNPshot	rs267606582
SNPdbe	rs267606582
MSV3d	rs267606582
GWAS Ctlg	rs267606582

Max Magnitude

0

ClinVar
Risk	rs267606582(-;-)
Alt	rs267606582(-;-)
Reference	Rs267606582(CAGG;CAGG)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258325_67258328delAGGC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034112.2,