rs267606539

Orientation

plus

Stabilized

plus

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

Make rs267606539(C;C)

Make rs267606539(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67487080

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606539
dbSNP (classic)	rs267606539
ClinGen	rs267606539
ebi	rs267606539
HLI	rs267606539
Exac	rs267606539
Gnomad	rs267606539
Varsome	rs267606539
LitVar	rs267606539
Map	rs267606539
PheGenI	rs267606539
Biobank	rs267606539
1000 genomes	rs267606539
hgdp	rs267606539
ensembl	rs267606539
geneview	rs267606539
scholar	rs267606539
google	rs267606539
pharmgkb	rs267606539
gwascentral	rs267606539
openSNP	rs267606539
23andMe	rs267606539
SNPshot	rs267606539
SNPdbe	rs267606539
MSV3d	rs267606539
GWAS Ctlg	rs267606539

Max Magnitude

0

ClinVar
Risk	rs267606539(C;C) rs267606539(T;T)
Alt	rs267606539(C;C) rs267606539(T;T)
Reference	Rs267606539(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma Familial Isolated Pituitary Adenomas
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma Familial Isolated Pituitary Adenomas
Reversed	0
HGVS	NC_000011.9:g.67254551G>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034065.2, RCV000383082.1,