rs104893763

Orientation

minus

Stabilized

minus

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

Make rs104893763(A;T)

Make rs104893763(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87264294

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893763
dbSNP (classic)	rs104893763
ClinGen	rs104893763
ebi	rs104893763
HLI	rs104893763
Exac	rs104893763
Gnomad	rs104893763
Varsome	rs104893763
LitVar	rs104893763
Map	rs104893763
PheGenI	rs104893763
Biobank	rs104893763
1000 genomes	rs104893763
hgdp	rs104893763
ensembl	rs104893763
geneview	rs104893763
scholar	rs104893763
google	rs104893763
pharmgkb	rs104893763
gwascentral	rs104893763
openSNP	rs104893763
23andMe	rs104893763
SNPshot	rs104893763
SNPdbe	rs104893763
MSV3d	rs104893763
GWAS Ctlg	rs104893763

Max Magnitude

0

OMIM	173110
Desc
Variant	0011
Related	also

ClinVar
Risk	rs104893763(T;T)
Alt	rs104893763(T;T)
Reference	Rs104893763(A;A)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	POU1F1
CLNDBN	Pituitary hormone deficiency, combined 1
Reversed	1
HGVS	NC_000003.11:g.87313444T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014582.27,