rs267606548

Orientation

plus

Stabilized

plus

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

Make rs267606548(A;G)

Make rs267606548(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489295

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606548
dbSNP (classic)	rs267606548
ClinGen	rs267606548
ebi	rs267606548
HLI	rs267606548
Exac	rs267606548
Gnomad	rs267606548
Varsome	rs267606548
LitVar	rs267606548
Map	rs267606548
PheGenI	rs267606548
Biobank	rs267606548
1000 genomes	rs267606548
hgdp	rs267606548
ensembl	rs267606548
geneview	rs267606548
scholar	rs267606548
google	rs267606548
pharmgkb	rs267606548
gwascentral	rs267606548
openSNP	rs267606548
23andMe	rs267606548
SNPshot	rs267606548
SNPdbe	rs267606548
MSV3d	rs267606548
GWAS Ctlg	rs267606548

Max Magnitude

0

ClinVar
Risk	rs267606548(G;G)
Alt	rs267606548(G;G)
Reference	Rs267606548(A;A)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256766A>G
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034073.2,