rs267606566

Orientation

plus

Stabilized

plus

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

Make rs267606566(C;T)

Make rs267606566(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490319

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606566
dbSNP (classic)	rs267606566
ClinGen	rs267606566
ebi	rs267606566
HLI	rs267606566
Exac	rs267606566
Gnomad	rs267606566
Varsome	rs267606566
LitVar	rs267606566
Map	rs267606566
PheGenI	rs267606566
Biobank	rs267606566
1000 genomes	rs267606566
hgdp	rs267606566
ensembl	rs267606566
geneview	rs267606566
scholar	rs267606566
google	rs267606566
pharmgkb	rs267606566
gwascentral	rs267606566
openSNP	rs267606566
23andMe	rs267606566
SNPshot	rs267606566
SNPdbe	rs267606566
MSV3d	rs267606566
GWAS Ctlg	rs267606566

Max Magnitude

0

ClinVar
Risk	rs267606566(T;T)
Alt	rs267606566(T;T)
Reference	Rs267606566(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257790C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034093.2,