rs104893766

Orientation

minus

Stabilized

minus

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

Make rs104893766(C;G)

Make rs104893766(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87262138

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893766
dbSNP (classic)	rs104893766
ClinGen	rs104893766
ebi	rs104893766
HLI	rs104893766
Exac	rs104893766
Gnomad	rs104893766
Varsome	rs104893766
LitVar	rs104893766
Map	rs104893766
PheGenI	rs104893766
Biobank	rs104893766
1000 genomes	rs104893766
hgdp	rs104893766
ensembl	rs104893766
geneview	rs104893766
scholar	rs104893766
google	rs104893766
pharmgkb	rs104893766
gwascentral	rs104893766
openSNP	rs104893766
23andMe	rs104893766
SNPshot	rs104893766
SNPdbe	rs104893766
MSV3d	rs104893766
GWAS Ctlg	rs104893766

Max Magnitude

0

OMIM	173110
Desc
Variant	0015
Related	also

ClinVar
Risk	rs104893766(G;G)
Alt	rs104893766(G;G)
Reference	Rs104893766(C;C)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	POU1F1
CLNDBN	Pituitary hormone deficiency, combined 1
Reversed	1
HGVS	NC_000003.11:g.87311288G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014586.27,