rs104893757

Orientation

minus

Stabilized

minus

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

Make rs104893757(C;T)

Make rs104893757(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87276392

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893757
dbSNP (classic)	rs104893757
ClinGen	rs104893757
ebi	rs104893757
HLI	rs104893757
Exac	rs104893757
Gnomad	rs104893757
Varsome	rs104893757
LitVar	rs104893757
Map	rs104893757
PheGenI	rs104893757
Biobank	rs104893757
1000 genomes	rs104893757
hgdp	rs104893757
ensembl	rs104893757
geneview	rs104893757
scholar	rs104893757
google	rs104893757
pharmgkb	rs104893757
gwascentral	rs104893757
openSNP	rs104893757
23andMe	rs104893757
SNPshot	rs104893757
SNPdbe	rs104893757
MSV3d	rs104893757
GWAS Ctlg	rs104893757

Max Magnitude

0

OMIM	173110
Desc
Variant	0004
Related	also

ClinVar
Risk	rs104893757(T;T)
Alt	rs104893757(T;T)
Reference	Rs104893757(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.87325542G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014575.20,