rs104893754

Orientation

minus

Stabilized

minus

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

Make rs104893754(C;T)

Make rs104893754(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87262161

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893754
dbSNP (classic)	rs104893754
ClinGen	rs104893754
ebi	rs104893754
HLI	rs104893754
Exac	rs104893754
Gnomad	rs104893754
Varsome	rs104893754
LitVar	rs104893754
Map	rs104893754
PheGenI	rs104893754
Biobank	rs104893754
1000 genomes	rs104893754
hgdp	rs104893754
ensembl	rs104893754
geneview	rs104893754
scholar	rs104893754
google	rs104893754
pharmgkb	rs104893754
gwascentral	rs104893754
openSNP	rs104893754
23andMe	rs104893754
SNPshot	rs104893754
SNPdbe	rs104893754
MSV3d	rs104893754
GWAS Ctlg	rs104893754

Max Magnitude

0

OMIM	173110
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893754(T;T)
Alt	rs104893754(T;T)
Reference	Rs104893754(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.87311311G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014572.25,