rs104894194

Orientation

plus

Stabilized

plus

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

Make rs104894194(C;T)

Make rs104894194(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483198

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs104894194
dbSNP (classic)	rs104894194
ClinGen	rs104894194
ebi	rs104894194
HLI	rs104894194
Exac	rs104894194
Gnomad	rs104894194
Varsome	rs104894194
LitVar	rs104894194
Map	rs104894194
PheGenI	rs104894194
Biobank	rs104894194
1000 genomes	rs104894194
hgdp	rs104894194
ensembl	rs104894194
geneview	rs104894194
scholar	rs104894194
google	rs104894194
pharmgkb	rs104894194
gwascentral	rs104894194
openSNP	rs104894194
23andMe	rs104894194
SNPshot	rs104894194
SNPdbe	rs104894194
MSV3d	rs104894194
GWAS Ctlg	rs104894194

Max Magnitude

0

OMIM	605555
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104894194(T;T)
Alt	rs104894194(T;T)
Reference	Rs104894194(C;C)
Significance	Pathogenic
Disease	Pituitary adenoma predisposition Prolactinoma Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Pituitary adenoma predisposition Prolactinoma, familial Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250669C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005163.3, RCV000005164.3, RCV000157603.3,