rs267606549

Orientation

plus

Stabilized

plus

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

Make rs267606549(-;-)

Make rs267606549(-;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489337

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606549
dbSNP (classic)	rs267606549
ClinGen	rs267606549
ebi	rs267606549
HLI	rs267606549
Exac	rs267606549
Gnomad	rs267606549
Varsome	rs267606549
LitVar	rs267606549
Map	rs267606549
PheGenI	rs267606549
Biobank	rs267606549
1000 genomes	rs267606549
hgdp	rs267606549
ensembl	rs267606549
geneview	rs267606549
scholar	rs267606549
google	rs267606549
pharmgkb	rs267606549
gwascentral	rs267606549
openSNP	rs267606549
23andMe	rs267606549
SNPshot	rs267606549
SNPdbe	rs267606549
MSV3d	rs267606549
GWAS Ctlg	rs267606549

Max Magnitude

0

ClinVar
Risk	rs267606549(-;-)
Alt	rs267606549(-;-)
Reference	Rs267606549(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256808delG
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034074.2,