rs267606581

Orientation

plus

Stabilized

plus

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

Make rs267606581(C;C)

Make rs267606581(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490829

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606581
dbSNP (classic)	rs267606581
ClinGen	rs267606581
ebi	rs267606581
HLI	rs267606581
Exac	rs267606581
Gnomad	rs267606581
Varsome	rs267606581
LitVar	rs267606581
Map	rs267606581
PheGenI	rs267606581
Biobank	rs267606581
1000 genomes	rs267606581
hgdp	rs267606581
ensembl	rs267606581
geneview	rs267606581
scholar	rs267606581
google	rs267606581
pharmgkb	rs267606581
gwascentral	rs267606581
openSNP	rs267606581
23andMe	rs267606581
SNPshot	rs267606581
SNPdbe	rs267606581
MSV3d	rs267606581
GWAS Ctlg	rs267606581

Max Magnitude

0

ClinVar
Risk	rs267606581(C;C)
Alt	rs267606581(C;C)
Reference	Rs267606581(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258300G>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034111.2,