rs267606583

Orientation

plus

Stabilized

plus

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

Make rs267606583(AG;GT)

Make rs267606583(GT;GT)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490878

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606583
dbSNP (classic)	rs267606583
ClinGen	rs267606583
ebi	rs267606583
HLI	rs267606583
Exac	rs267606583
Gnomad	rs267606583
Varsome	rs267606583
LitVar	rs267606583
Map	rs267606583
PheGenI	rs267606583
Biobank	rs267606583
1000 genomes	rs267606583
hgdp	rs267606583
ensembl	rs267606583
geneview	rs267606583
scholar	rs267606583
google	rs267606583
pharmgkb	rs267606583
gwascentral	rs267606583
openSNP	rs267606583
23andMe	rs267606583
SNPshot	rs267606583
SNPdbe	rs267606583
MSV3d	rs267606583
GWAS Ctlg	rs267606583

Max Magnitude

0

ClinVar
Risk	rs267606583(GT;GT)
Alt	rs267606583(GT;GT)
Reference	Rs267606583(AG;AG)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258349_67258350delAGinsGT
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034118.2,