rs267606551

Orientation

plus

Stabilized

plus

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

Make rs267606551(-;-)

Make rs267606551(-;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489391

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606551
dbSNP (classic)	rs267606551
ClinGen	rs267606551
ebi	rs267606551
HLI	rs267606551
Exac	rs267606551
Gnomad	rs267606551
Varsome	rs267606551
LitVar	rs267606551
Map	rs267606551
PheGenI	rs267606551
Biobank	rs267606551
1000 genomes	rs267606551
hgdp	rs267606551
ensembl	rs267606551
geneview	rs267606551
scholar	rs267606551
google	rs267606551
pharmgkb	rs267606551
gwascentral	rs267606551
openSNP	rs267606551
23andMe	rs267606551
SNPshot	rs267606551
SNPdbe	rs267606551
MSV3d	rs267606551
GWAS Ctlg	rs267606551

Max Magnitude

0

ClinVar
Risk	rs267606551(-;-)
Alt	rs267606551(-;-)
Reference	Rs267606551(A;A)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256862delA
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034077.2,