rs267606569

Orientation

plus

Stabilized

plus

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

Make rs267606569(A;A)

Make rs267606569(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490383

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606569
dbSNP (classic)	rs267606569
ClinGen	rs267606569
ebi	rs267606569
HLI	rs267606569
Exac	rs267606569
Gnomad	rs267606569
Varsome	rs267606569
LitVar	rs267606569
Map	rs267606569
PheGenI	rs267606569
Biobank	rs267606569
1000 genomes	rs267606569
hgdp	rs267606569
ensembl	rs267606569
geneview	rs267606569
scholar	rs267606569
google	rs267606569
pharmgkb	rs267606569
gwascentral	rs267606569
openSNP	rs267606569
23andMe	rs267606569
SNPshot	rs267606569
SNPdbe	rs267606569
MSV3d	rs267606569
GWAS Ctlg	rs267606569

Max Magnitude

0

ClinVar
Risk	rs267606569(A;A)
Alt	rs267606569(A;A)
Reference	Rs267606569(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257854G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034096.2,