rs267606577

Orientation

plus

Stabilized

plus

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

Make rs267606577(A;G)

Make rs267606577(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490803

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606577
dbSNP (classic)	rs267606577
ClinGen	rs267606577
ebi	rs267606577
HLI	rs267606577
Exac	rs267606577
Gnomad	rs267606577
Varsome	rs267606577
LitVar	rs267606577
Map	rs267606577
PheGenI	rs267606577
Biobank	rs267606577
1000 genomes	rs267606577
hgdp	rs267606577
ensembl	rs267606577
geneview	rs267606577
scholar	rs267606577
google	rs267606577
pharmgkb	rs267606577
gwascentral	rs267606577
openSNP	rs267606577
23andMe	rs267606577
SNPshot	rs267606577
SNPdbe	rs267606577
MSV3d	rs267606577
GWAS Ctlg	rs267606577

Max Magnitude

0

ClinVar
Risk	rs267606577(G;G)
Alt	rs267606577(G;G)
Reference	Rs267606577(A;A)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258274A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034105.2,