rs267606547

Orientation

plus

Stabilized

plus

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

Make rs267606547(-;C)

Make rs267606547(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483161

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606547
dbSNP (classic)	rs267606547
ClinGen	rs267606547
ebi	rs267606547
HLI	rs267606547
Exac	rs267606547
Gnomad	rs267606547
Varsome	rs267606547
LitVar	rs267606547
Map	rs267606547
PheGenI	rs267606547
Biobank	rs267606547
1000 genomes	rs267606547
hgdp	rs267606547
ensembl	rs267606547
geneview	rs267606547
scholar	rs267606547
google	rs267606547
pharmgkb	rs267606547
gwascentral	rs267606547
openSNP	rs267606547
23andMe	rs267606547
SNPshot	rs267606547
SNPdbe	rs267606547
MSV3d	rs267606547
GWAS Ctlg	rs267606547

Max Magnitude

0

ClinVar
Risk	rs267606547(C;C)
Alt	rs267606547(C;C)
Reference	Rs267606547(-;-)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250632_67250633insC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034076.2,