rs104895072

Orientation

plus

Stabilized

plus

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

Make rs104895072(G;T)

Make rs104895072(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67487155

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs104895072
dbSNP (classic)	rs104895072
ClinGen	rs104895072
ebi	rs104895072
HLI	rs104895072
Exac	rs104895072
Gnomad	rs104895072
Varsome	rs104895072
LitVar	rs104895072
Map	rs104895072
PheGenI	rs104895072
Biobank	rs104895072
1000 genomes	rs104895072
hgdp	rs104895072
ensembl	rs104895072
geneview	rs104895072
scholar	rs104895072
google	rs104895072
pharmgkb	rs104895072
gwascentral	rs104895072
openSNP	rs104895072
23andMe	rs104895072
SNPshot	rs104895072
SNPdbe	rs104895072
MSV3d	rs104895072
GWAS Ctlg	rs104895072

Max Magnitude

0

ClinVar
Risk	rs104895072(T;T)
Alt	rs104895072(T;T)
Reference	Rs104895072(G;G)
Significance	Probable-Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67254626G>T
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034068.2,