rs104893764

Orientation

minus

Stabilized

minus

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

Make rs104893764(A;A)

Make rs104893764(A;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87260082

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893764
dbSNP (classic)	rs104893764
ClinGen	rs104893764
ebi	rs104893764
HLI	rs104893764
Exac	rs104893764
Gnomad	rs104893764
Varsome	rs104893764
LitVar	rs104893764
Map	rs104893764
PheGenI	rs104893764
Biobank	rs104893764
1000 genomes	rs104893764
hgdp	rs104893764
ensembl	rs104893764
geneview	rs104893764
scholar	rs104893764
google	rs104893764
pharmgkb	rs104893764
gwascentral	rs104893764
openSNP	rs104893764
23andMe	rs104893764
SNPshot	rs104893764
SNPdbe	rs104893764
MSV3d	rs104893764
GWAS Ctlg	rs104893764

Max Magnitude

0

OMIM	173110
Desc
Variant	0012
Related	also

ClinVar
Risk	rs104893764(A;A)
Alt	rs104893764(A;A)
Reference	Rs104893764(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.87309232C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014583.26,