rs267606557

Orientation

plus

Stabilized

plus

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

Make rs267606557(-;-)

Make rs267606557(-;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490069

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606557
dbSNP (classic)	rs267606557
ClinGen	rs267606557
ebi	rs267606557
HLI	rs267606557
Exac	rs267606557
Gnomad	rs267606557
Varsome	rs267606557
LitVar	rs267606557
Map	rs267606557
PheGenI	rs267606557
Biobank	rs267606557
1000 genomes	rs267606557
hgdp	rs267606557
ensembl	rs267606557
geneview	rs267606557
scholar	rs267606557
google	rs267606557
pharmgkb	rs267606557
gwascentral	rs267606557
openSNP	rs267606557
23andMe	rs267606557
SNPshot	rs267606557
SNPdbe	rs267606557
MSV3d	rs267606557
GWAS Ctlg	rs267606557

Max Magnitude

0

ClinVar
Risk	rs267606557(-;-)
Alt	rs267606557(-;-)
Reference	Rs267606557(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257540delC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034085.2,