rs267606563

Orientation

plus

Stabilized

plus

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

Make rs267606563(A;T)

Make rs267606563(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490170

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606563
dbSNP (classic)	rs267606563
ClinGen	rs267606563
ebi	rs267606563
HLI	rs267606563
Exac	rs267606563
Gnomad	rs267606563
Varsome	rs267606563
LitVar	rs267606563
Map	rs267606563
PheGenI	rs267606563
Biobank	rs267606563
1000 genomes	rs267606563
hgdp	rs267606563
ensembl	rs267606563
geneview	rs267606563
scholar	rs267606563
google	rs267606563
pharmgkb	rs267606563
gwascentral	rs267606563
openSNP	rs267606563
23andMe	rs267606563
SNPshot	rs267606563
SNPdbe	rs267606563
MSV3d	rs267606563
GWAS Ctlg	rs267606563

Max Magnitude

0

ClinVar
Risk	rs267606563(T;T)
Alt	rs267606563(T;T)
Reference	Rs267606563(A;A)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257641A>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034090.2,