rs104893755

Orientation

minus

Stabilized

minus

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

Make rs104893755(C;T)

Make rs104893755(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87259959

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893755
dbSNP (classic)	rs104893755
ClinGen	rs104893755
ebi	rs104893755
HLI	rs104893755
Exac	rs104893755
Gnomad	rs104893755
Varsome	rs104893755
LitVar	rs104893755
Map	rs104893755
PheGenI	rs104893755
Biobank	rs104893755
1000 genomes	rs104893755
hgdp	rs104893755
ensembl	rs104893755
geneview	rs104893755
scholar	rs104893755
google	rs104893755
pharmgkb	rs104893755
gwascentral	rs104893755
openSNP	rs104893755
23andMe	rs104893755
SNPshot	rs104893755
SNPdbe	rs104893755
MSV3d	rs104893755
GWAS Ctlg	rs104893755

Max Magnitude

0

OMIM	173110
Desc
Variant	0002
Related	also

ClinVar
Risk	rs104893755(T;T)
Alt	rs104893755(T;T)
Reference	Rs104893755(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.87309109G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014573.26,