rs267606552

Orientation

plus

Stabilized

plus

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

Make rs267606552(C;T)

Make rs267606552(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489411

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606552
dbSNP (classic)	rs267606552
ClinGen	rs267606552
ebi	rs267606552
HLI	rs267606552
Exac	rs267606552
Gnomad	rs267606552
Varsome	rs267606552
LitVar	rs267606552
Map	rs267606552
PheGenI	rs267606552
Biobank	rs267606552
1000 genomes	rs267606552
hgdp	rs267606552
ensembl	rs267606552
geneview	rs267606552
scholar	rs267606552
google	rs267606552
pharmgkb	rs267606552
gwascentral	rs267606552
openSNP	rs267606552
23andMe	rs267606552
SNPshot	rs267606552
SNPdbe	rs267606552
MSV3d	rs267606552
GWAS Ctlg	rs267606552

Max Magnitude

0

ClinVar
Risk	rs267606552(T;T)
Alt	rs267606552(T;T)
Reference	Rs267606552(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256882C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034078.2,