rs267606565

Orientation

plus

Stabilized

plus

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

Make rs267606565(G;T)

Make rs267606565(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490316

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606565
dbSNP (classic)	rs267606565
ClinGen	rs267606565
ebi	rs267606565
HLI	rs267606565
Exac	rs267606565
Gnomad	rs267606565
Varsome	rs267606565
LitVar	rs267606565
Map	rs267606565
PheGenI	rs267606565
Biobank	rs267606565
1000 genomes	rs267606565
hgdp	rs267606565
ensembl	rs267606565
geneview	rs267606565
scholar	rs267606565
google	rs267606565
pharmgkb	rs267606565
gwascentral	rs267606565
openSNP	rs267606565
23andMe	rs267606565
SNPshot	rs267606565
SNPdbe	rs267606565
MSV3d	rs267606565
GWAS Ctlg	rs267606565

Max Magnitude

0

ClinVar
Risk	rs267606565(T;T)
Alt	rs267606565(T;T)
Reference	Rs267606565(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257787G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034092.2,