rs267606554

Orientation

plus

Stabilized

plus

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

Make rs267606554(A;A)

Make rs267606554(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489456

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606554
dbSNP (classic)	rs267606554
ClinGen	rs267606554
ebi	rs267606554
HLI	rs267606554
Exac	rs267606554
Gnomad	rs267606554
Varsome	rs267606554
LitVar	rs267606554
Map	rs267606554
PheGenI	rs267606554
Biobank	rs267606554
1000 genomes	rs267606554
hgdp	rs267606554
ensembl	rs267606554
geneview	rs267606554
scholar	rs267606554
google	rs267606554
pharmgkb	rs267606554
gwascentral	rs267606554
openSNP	rs267606554
23andMe	rs267606554
SNPshot	rs267606554
SNPdbe	rs267606554
MSV3d	rs267606554
GWAS Ctlg	rs267606554

Max Magnitude

0

ClinVar
Risk	rs267606554(A;A)
Alt	rs267606554(A;A)
Reference	Rs267606554(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256927G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034081.2,