rs267606568

Orientation

plus

Stabilized

plus

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

Make rs267606568(G;T)

Make rs267606568(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483228

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606568
dbSNP (classic)	rs267606568
ClinGen	rs267606568
ebi	rs267606568
HLI	rs267606568
Exac	rs267606568
Gnomad	rs267606568
Varsome	rs267606568
LitVar	rs267606568
Map	rs267606568
PheGenI	rs267606568
Biobank	rs267606568
1000 genomes	rs267606568
hgdp	rs267606568
ensembl	rs267606568
geneview	rs267606568
scholar	rs267606568
google	rs267606568
pharmgkb	rs267606568
gwascentral	rs267606568
openSNP	rs267606568
23andMe	rs267606568
SNPshot	rs267606568
SNPdbe	rs267606568
MSV3d	rs267606568
GWAS Ctlg	rs267606568

Max Magnitude

0

ClinVar
Risk	rs267606568(C;C) rs267606568(T;T)
Alt	rs267606568(C;C) rs267606568(T;T)
Reference	Rs267606568(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250699G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034095.2,