rs104893765

Orientation

minus

Stabilized

minus

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

Make rs104893765(A;A)

Make rs104893765(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87262160

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893765
dbSNP (classic)	rs104893765
ClinGen	rs104893765
ebi	rs104893765
HLI	rs104893765
Exac	rs104893765
Gnomad	rs104893765
Varsome	rs104893765
LitVar	rs104893765
Map	rs104893765
PheGenI	rs104893765
Biobank	rs104893765
1000 genomes	rs104893765
hgdp	rs104893765
ensembl	rs104893765
geneview	rs104893765
scholar	rs104893765
google	rs104893765
pharmgkb	rs104893765
gwascentral	rs104893765
openSNP	rs104893765
23andMe	rs104893765
SNPshot	rs104893765
SNPdbe	rs104893765
MSV3d	rs104893765
GWAS Ctlg	rs104893765

Max Magnitude

0

OMIM	173110
Desc
Variant	0013
Related	also

ClinVar
Risk	rs104893765(A;A)
Alt	rs104893765(A;A)
Reference	Rs104893765(G;G)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	POU1F1
CLNDBN	Pituitary hormone deficiency, combined 1
Reversed	1
HGVS	NC_000003.11:g.87311310C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014584.25,