rs104895074

Orientation

plus

Stabilized

plus

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

Make rs104895074(CCCCGAT;CCCCGAT)

Make rs104895074(CCCCGAT;TCCCGGAC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67483232

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs104895074
dbSNP (classic)	rs104895074
ClinGen	rs104895074
ebi	rs104895074
HLI	rs104895074
Exac	rs104895074
Gnomad	rs104895074
Varsome	rs104895074
LitVar	rs104895074
Map	rs104895074
PheGenI	rs104895074
Biobank	rs104895074
1000 genomes	rs104895074
hgdp	rs104895074
ensembl	rs104895074
geneview	rs104895074
scholar	rs104895074
google	rs104895074
pharmgkb	rs104895074
gwascentral	rs104895074
openSNP	rs104895074
23andMe	rs104895074
SNPshot	rs104895074
SNPdbe	rs104895074
MSV3d	rs104895074
GWAS Ctlg	rs104895074

Max Magnitude

0

ClinVar
Risk	rs104895074(CCCCGAT;CCCCGAT)
Alt	rs104895074(CCCCGAT;CCCCGAT)
Reference	Rs104895074(TCCCGGAC;TCCCGGAC)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67250703_67250710delTCCCGGACinsCCCCGAT
CLNSRC
CLNACC