rs267606571

Orientation

plus

Stabilized

plus

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

Make rs267606571(C;T)

Make rs267606571(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490385

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606571
dbSNP (classic)	rs267606571
ClinGen	rs267606571
ebi	rs267606571
HLI	rs267606571
Exac	rs267606571
Gnomad	rs267606571
Varsome	rs267606571
LitVar	rs267606571
Map	rs267606571
PheGenI	rs267606571
Biobank	rs267606571
1000 genomes	rs267606571
hgdp	rs267606571
ensembl	rs267606571
geneview	rs267606571
scholar	rs267606571
google	rs267606571
pharmgkb	rs267606571
gwascentral	rs267606571
openSNP	rs267606571
23andMe	rs267606571
SNPshot	rs267606571
SNPdbe	rs267606571
MSV3d	rs267606571
GWAS Ctlg	rs267606571

Max Magnitude

0

ClinVar
Risk	rs267606571(T;T)
Alt	rs267606571(T;T)
Reference	Rs267606571(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257856C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034098.2,