rs104894195

Orientation

plus

Stabilized

plus

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

Make rs104894195(C;T)

Make rs104894195(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490910

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs104894195
dbSNP (classic)	rs104894195
ClinGen	rs104894195
ebi	rs104894195
HLI	rs104894195
Exac	rs104894195
Gnomad	rs104894195
Varsome	rs104894195
LitVar	rs104894195
Map	rs104894195
PheGenI	rs104894195
Biobank	rs104894195
1000 genomes	rs104894195
hgdp	rs104894195
ensembl	rs104894195
geneview	rs104894195
scholar	rs104894195
google	rs104894195
pharmgkb	rs104894195
gwascentral	rs104894195
openSNP	rs104894195
23andMe	rs104894195
SNPshot	rs104894195
SNPdbe	rs104894195
MSV3d	rs104894195
GWAS Ctlg	rs104894195

Max Magnitude

0

OMIM	605555
Desc
Variant	0003
Related	also

ClinVar
Risk	rs104894195(G;G) rs104894195(T;T)
Alt	rs104894195(G;G) rs104894195(T;T)
Reference	Rs104894195(C;C)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258381C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005166.3,