rs267606546

Orientation

plus

Stabilized

plus

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

Make rs267606546(C;C)

Make rs267606546(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483160

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606546
dbSNP (classic)	rs267606546
ClinGen	rs267606546
ebi	rs267606546
HLI	rs267606546
Exac	rs267606546
Gnomad	rs267606546
Varsome	rs267606546
LitVar	rs267606546
Map	rs267606546
PheGenI	rs267606546
Biobank	rs267606546
1000 genomes	rs267606546
hgdp	rs267606546
ensembl	rs267606546
geneview	rs267606546
scholar	rs267606546
google	rs267606546
pharmgkb	rs267606546
gwascentral	rs267606546
openSNP	rs267606546
23andMe	rs267606546
SNPshot	rs267606546
SNPdbe	rs267606546
MSV3d	rs267606546
GWAS Ctlg	rs267606546

Max Magnitude

0

ClinVar
Risk	rs267606546(C;C)
Alt	rs267606546(C;C)
Reference	Rs267606546(T;T)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250631T>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034072.2,