rs267606578

Orientation

plus

Stabilized

plus

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

Make rs267606578(-;TTCAAGCGGGGCAAGGCCCAC)

Make rs267606578(TTCAAGCGGGGCAAGGCCCAC;TTCAAGCGGGGCAAGGCCCAC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

67490825

Gene

AIP

is a	snp
is	mentioned by
dbSNP	rs267606578
dbSNP (classic)	rs267606578
ClinGen	rs267606578
ebi	rs267606578
HLI	rs267606578
Exac	rs267606578
Gnomad	rs267606578
Varsome	rs267606578
LitVar	rs267606578
Map	rs267606578
PheGenI	rs267606578
Biobank	rs267606578
1000 genomes	rs267606578
hgdp	rs267606578
ensembl	rs267606578
geneview	rs267606578
scholar	rs267606578
google	rs267606578
pharmgkb	rs267606578
gwascentral	rs267606578
openSNP	rs267606578
23andMe	rs267606578
SNPshot	rs267606578
SNPdbe	rs267606578
MSV3d	rs267606578
GWAS Ctlg	rs267606578

Max Magnitude

0

ClinVar
Risk	rs267606578(ACTTCAAGCGGGGCAAGGCCC;ACTTCAAGCGGGGCAAGGCCC)
Alt	rs267606578(ACTTCAAGCGGGGCAAGGCCC;ACTTCAAGCGGGGCAAGGCCC)
Reference	Rs267606578(-;-)
Significance	Pathogenic
Disease	Somatotroph adenoma
Variation	info
Gene	AIP
CLNDBN	Somatotroph adenoma
Reversed	0
HGVS	NC_000011.9:g.67258276_67258296dup21
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000034107.2,