rs267606556

Orientation

plus

Stabilized

plus

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

Make rs267606556(A;G)

Make rs267606556(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490036

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606556
dbSNP (classic)	rs267606556
ClinGen	rs267606556
ebi	rs267606556
HLI	rs267606556
Exac	rs267606556
Gnomad	rs267606556
Varsome	rs267606556
LitVar	rs267606556
Map	rs267606556
PheGenI	rs267606556
Biobank	rs267606556
1000 genomes	rs267606556
hgdp	rs267606556
ensembl	rs267606556
geneview	rs267606556
scholar	rs267606556
google	rs267606556
pharmgkb	rs267606556
gwascentral	rs267606556
openSNP	rs267606556
23andMe	rs267606556
SNPshot	rs267606556
SNPdbe	rs267606556
MSV3d	rs267606556
GWAS Ctlg	rs267606556

Max Magnitude

0

ClinVar
Risk	rs267606556(G;G)
Alt	rs267606556(G;G)
Reference	Rs267606556(A;A)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257507A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034082.2,