rs104895073

Orientation

plus

Stabilized

plus

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

Make rs104895073(C;T)

Make rs104895073(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490059

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs104895073
dbSNP (classic)	rs104895073
ClinGen	rs104895073
ebi	rs104895073
HLI	rs104895073
Exac	rs104895073
Gnomad	rs104895073
Varsome	rs104895073
LitVar	rs104895073
Map	rs104895073
PheGenI	rs104895073
Biobank	rs104895073
1000 genomes	rs104895073
hgdp	rs104895073
ensembl	rs104895073
geneview	rs104895073
scholar	rs104895073
google	rs104895073
pharmgkb	rs104895073
gwascentral	rs104895073
openSNP	rs104895073
23andMe	rs104895073
SNPshot	rs104895073
SNPdbe	rs104895073
MSV3d	rs104895073
GWAS Ctlg	rs104895073

Max Magnitude

0

ClinVar
Risk	rs104895073(T;T)
Alt	rs104895073(T;T)
Reference	Rs104895073(C;C)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67257530C>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034084.2,