rs202006716

Orientation

plus

Stabilized

plus

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

Make rs202006716(A;A)

Make rs202006716(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490160

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs202006716
dbSNP (classic)	rs202006716
ClinGen	rs202006716
ebi	rs202006716
HLI	rs202006716
Exac	rs202006716
Gnomad	rs202006716
Varsome	rs202006716
LitVar	rs202006716
Map	rs202006716
PheGenI	rs202006716
Biobank	rs202006716
1000 genomes	rs202006716
hgdp	rs202006716
ensembl	rs202006716
geneview	rs202006716
scholar	rs202006716
google	rs202006716
pharmgkb	rs202006716
gwascentral	rs202006716
openSNP	rs202006716
23andMe	rs202006716
SNPshot	rs202006716
SNPdbe	rs202006716
MSV3d	rs202006716
GWAS Ctlg	rs202006716

Max Magnitude

0

ClinVar
Risk	rs202006716(A;A)
Alt	rs202006716(A;A)
Reference	Rs202006716(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257631G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034089.2,