rs104893761

Orientation

minus

Stabilized

minus

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

Make rs104893761(G;G)

Make rs104893761(G;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87264323

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893761
dbSNP (classic)	rs104893761
ClinGen	rs104893761
ebi	rs104893761
HLI	rs104893761
Exac	rs104893761
Gnomad	rs104893761
Varsome	rs104893761
LitVar	rs104893761
Map	rs104893761
PheGenI	rs104893761
Biobank	rs104893761
1000 genomes	rs104893761
hgdp	rs104893761
ensembl	rs104893761
geneview	rs104893761
scholar	rs104893761
google	rs104893761
pharmgkb	rs104893761
gwascentral	rs104893761
openSNP	rs104893761
23andMe	rs104893761
SNPshot	rs104893761
SNPdbe	rs104893761
MSV3d	rs104893761
GWAS Ctlg	rs104893761

Max Magnitude

0

OMIM	173110
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104893761(G;G)
Alt	rs104893761(G;G)
Reference	Rs104893761(T;T)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	POU1F1
CLNDBN	Pituitary hormone deficiency, combined 1
Reversed	1
HGVS	NC_000003.11:g.87313473A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014578.27,