rs267606561

Orientation

plus

Stabilized

plus

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

Make rs267606561(C;C)

Make rs267606561(C;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490153

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606561
dbSNP (classic)	rs267606561
ClinGen	rs267606561
ebi	rs267606561
HLI	rs267606561
Exac	rs267606561
Gnomad	rs267606561
Varsome	rs267606561
LitVar	rs267606561
Map	rs267606561
PheGenI	rs267606561
Biobank	rs267606561
1000 genomes	rs267606561
hgdp	rs267606561
ensembl	rs267606561
geneview	rs267606561
scholar	rs267606561
google	rs267606561
pharmgkb	rs267606561
gwascentral	rs267606561
openSNP	rs267606561
23andMe	rs267606561
SNPshot	rs267606561
SNPdbe	rs267606561
MSV3d	rs267606561
GWAS Ctlg	rs267606561

Max Magnitude

0

ClinVar
Risk	rs267606561(C;C)
Alt	rs267606561(C;C)
Reference	Rs267606561(T;T)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257624T>C
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034088.2,