rs104895075

Orientation

plus

Stabilized

plus

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

Make rs104895075(-;C)

Make rs104895075(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490332

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs104895075
dbSNP (classic)	rs104895075
ClinGen	rs104895075
ebi	rs104895075
HLI	rs104895075
Exac	rs104895075
Gnomad	rs104895075
Varsome	rs104895075
LitVar	rs104895075
Map	rs104895075
PheGenI	rs104895075
Biobank	rs104895075
1000 genomes	rs104895075
hgdp	rs104895075
ensembl	rs104895075
geneview	rs104895075
scholar	rs104895075
google	rs104895075
pharmgkb	rs104895075
gwascentral	rs104895075
openSNP	rs104895075
23andMe	rs104895075
SNPshot	rs104895075
SNPdbe	rs104895075
MSV3d	rs104895075
GWAS Ctlg	rs104895075

Max Magnitude

0

ClinVar
Risk	rs104895075(C;C)
Alt	rs104895075(C;C)
Reference	Rs104895075(-;-)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257803dupC
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034094.3,