rs267606579

Orientation

plus

Stabilized

plus

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

Make rs267606579(C;T)

Make rs267606579(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490811

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606579
dbSNP (classic)	rs267606579
ClinGen	rs267606579
ebi	rs267606579
HLI	rs267606579
Exac	rs267606579
Gnomad	rs267606579
Varsome	rs267606579
LitVar	rs267606579
Map	rs267606579
PheGenI	rs267606579
Biobank	rs267606579
1000 genomes	rs267606579
hgdp	rs267606579
ensembl	rs267606579
geneview	rs267606579
scholar	rs267606579
google	rs267606579
pharmgkb	rs267606579
gwascentral	rs267606579
openSNP	rs267606579
23andMe	rs267606579
SNPshot	rs267606579
SNPdbe	rs267606579
MSV3d	rs267606579
GWAS Ctlg	rs267606579

Max Magnitude

0

ClinVar
Risk	rs267606579(T;T)
Alt	rs267606579(T;T)
Reference	Rs267606579(C;C)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258282C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034109.2,