rs267606545

Orientation

plus

Stabilized

plus

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

Make rs267606545(-;-)

Make rs267606545(-;GT)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67489273

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606545
dbSNP (classic)	rs267606545
ClinGen	rs267606545
ebi	rs267606545
HLI	rs267606545
Exac	rs267606545
Gnomad	rs267606545
Varsome	rs267606545
LitVar	rs267606545
Map	rs267606545
PheGenI	rs267606545
Biobank	rs267606545
1000 genomes	rs267606545
hgdp	rs267606545
ensembl	rs267606545
geneview	rs267606545
scholar	rs267606545
google	rs267606545
pharmgkb	rs267606545
gwascentral	rs267606545
openSNP	rs267606545
23andMe	rs267606545
SNPshot	rs267606545
SNPdbe	rs267606545
MSV3d	rs267606545
GWAS Ctlg	rs267606545

Max Magnitude

0

ClinVar
Risk	rs267606545(-;-)
Alt	rs267606545(-;-)
Reference	Rs267606545(GT;GT)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67256744_67256745delGT
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034071.2,