rs121908356

Orientation

plus

Stabilized

plus

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

Make rs121908356(A;A)

Make rs121908356(A;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490804

Gene	AIP, MIR6752

is a	snp
is	mentioned by
dbSNP	rs121908356
dbSNP (classic)	rs121908356
ClinGen	rs121908356
ebi	rs121908356
HLI	rs121908356
Exac	rs121908356
Gnomad	rs121908356
Varsome	rs121908356
LitVar	rs121908356
Map	rs121908356
PheGenI	rs121908356
Biobank	rs121908356
1000 genomes	rs121908356
hgdp	rs121908356
ensembl	rs121908356
geneview	rs121908356
scholar	rs121908356
google	rs121908356
pharmgkb	rs121908356
gwascentral	rs121908356
openSNP	rs121908356
23andMe	rs121908356
SNPshot	rs121908356
SNPdbe	rs121908356
MSV3d	rs121908356
GWAS Ctlg	rs121908356

Max Magnitude

0

OMIM	605555
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121908356(A;A)
Alt	rs121908356(A;A)
Reference	Rs121908356(C;C)
Significance	Pathogenic
Disease	Pituitary adenoma predisposition Somatotroph adenoma
Variation	info
Gene	MIR6752 AIP
CLNDBN	Pituitary adenoma predisposition Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258275C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005170.3, RCV000034106.2,