rs267606541

Orientation

plus

Stabilized

plus

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

Make rs267606541(C;T)

Make rs267606541(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67487147

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606541
dbSNP (classic)	rs267606541
ClinGen	rs267606541
ebi	rs267606541
HLI	rs267606541
Exac	rs267606541
Gnomad	rs267606541
Varsome	rs267606541
LitVar	rs267606541
Map	rs267606541
PheGenI	rs267606541
Biobank	rs267606541
1000 genomes	rs267606541
hgdp	rs267606541
ensembl	rs267606541
geneview	rs267606541
scholar	rs267606541
google	rs267606541
pharmgkb	rs267606541
gwascentral	rs267606541
openSNP	rs267606541
23andMe	rs267606541
SNPshot	rs267606541
SNPdbe	rs267606541
MSV3d	rs267606541
GWAS Ctlg	rs267606541

Max Magnitude

0

ClinVar
Risk	rs267606541(T;T)
Alt	rs267606541(T;T)
Reference	Rs267606541(C;C)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67254618C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034066.2,