rs267606544

Orientation

plus

Stabilized

plus

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

Make rs267606544(A;A)

Make rs267606544(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489266

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606544
dbSNP (classic)	rs267606544
ClinGen	rs267606544
ebi	rs267606544
HLI	rs267606544
Exac	rs267606544
Gnomad	rs267606544
Varsome	rs267606544
LitVar	rs267606544
Map	rs267606544
PheGenI	rs267606544
Biobank	rs267606544
1000 genomes	rs267606544
hgdp	rs267606544
ensembl	rs267606544
geneview	rs267606544
scholar	rs267606544
google	rs267606544
pharmgkb	rs267606544
gwascentral	rs267606544
openSNP	rs267606544
23andMe	rs267606544
SNPshot	rs267606544
SNPdbe	rs267606544
MSV3d	rs267606544
GWAS Ctlg	rs267606544

Max Magnitude

0

ClinVar
Risk	rs267606544(A;A)
Alt	rs267606544(A;A)
Reference	Rs267606544(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256737G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034070.2,