rs121908357

Orientation

plus

Stabilized

plus

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

Make rs121908357(C;T)

Make rs121908357(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483222

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs121908357
dbSNP (classic)	rs121908357
ClinGen	rs121908357
ebi	rs121908357
HLI	rs121908357
Exac	rs121908357
Gnomad	rs121908357
Varsome	rs121908357
LitVar	rs121908357
Map	rs121908357
PheGenI	rs121908357
Biobank	rs121908357
1000 genomes	rs121908357
hgdp	rs121908357
ensembl	rs121908357
geneview	rs121908357
scholar	rs121908357
google	rs121908357
pharmgkb	rs121908357
gwascentral	rs121908357
openSNP	rs121908357
23andMe	rs121908357
SNPshot	rs121908357
SNPdbe	rs121908357
MSV3d	rs121908357
GWAS Ctlg	rs121908357

Max Magnitude

0

OMIM	605555
Desc
Variant	0009
Related	also

ClinVar
Risk	rs121908357(T;T)
Alt	rs121908357(T;T)
Reference	Rs121908357(C;C)
Significance	Other
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250693C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005172.5,