rs104894190

Orientation

plus

Stabilized

plus

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

Make rs104894190(A;A)

Make rs104894190(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490911

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs104894190
dbSNP (classic)	rs104894190
ClinGen	rs104894190
ebi	rs104894190
HLI	rs104894190
Exac	rs104894190
Gnomad	rs104894190
Varsome	rs104894190
LitVar	rs104894190
Map	rs104894190
PheGenI	rs104894190
Biobank	rs104894190
1000 genomes	rs104894190
hgdp	rs104894190
ensembl	rs104894190
geneview	rs104894190
scholar	rs104894190
google	rs104894190
pharmgkb	rs104894190
gwascentral	rs104894190
openSNP	rs104894190
23andMe	rs104894190
SNPshot	rs104894190
SNPdbe	rs104894190
MSV3d	rs104894190
GWAS Ctlg	rs104894190

Max Magnitude

0

OMIM	605555
Desc
Variant	0008
Related	also

ClinVar
Risk	rs104894190(A;A)
Alt	rs104894190(A;A)
Reference	Rs104894190(G;G)
Significance	Pathogenic
Disease	Pituitary dependent hypercortisolism Familial Isolated Pituitary Adenomas not specified
Variation	info
Gene	AIP
CLNDBN	Pituitary dependent hypercortisolism Familial Isolated Pituitary Adenomas not specified
Reversed	0
HGVS	NC_000011.9:g.67258382G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005171.1, RCV000408430.1, RCV000439236.1,