rs267606573

Orientation

plus

Stabilized

plus

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

Make rs267606573(A;G)

Make rs267606573(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490391

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs267606573
dbSNP (classic)	rs267606573
ClinGen	rs267606573
ebi	rs267606573
HLI	rs267606573
Exac	rs267606573
Gnomad	rs267606573
Varsome	rs267606573
LitVar	rs267606573
Map	rs267606573
PheGenI	rs267606573
Biobank	rs267606573
1000 genomes	rs267606573
hgdp	rs267606573
ensembl	rs267606573
geneview	rs267606573
scholar	rs267606573
google	rs267606573
pharmgkb	rs267606573
gwascentral	rs267606573
openSNP	rs267606573
23andMe	rs267606573
SNPshot	rs267606573
SNPdbe	rs267606573
MSV3d	rs267606573
GWAS Ctlg	rs267606573

Max Magnitude

0

ClinVar
Risk	rs267606573(G;G) rs267606573(T;T)
Alt	rs267606573(G;G) rs267606573(T;T)
Reference	Rs267606573(A;A)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257862A>G; NC_000011.9:g.67257862A>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034099.2, RCV000034100.2,