rs104893760

Orientation

minus

Stabilized

minus

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

Make rs104893760(G;T)

Make rs104893760(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

87260022

Gene

POU1F1

is a	snp
is	mentioned by
dbSNP	rs104893760
dbSNP (classic)	rs104893760
ClinGen	rs104893760
ebi	rs104893760
HLI	rs104893760
Exac	rs104893760
Gnomad	rs104893760
Varsome	rs104893760
LitVar	rs104893760
Map	rs104893760
PheGenI	rs104893760
Biobank	rs104893760
1000 genomes	rs104893760
hgdp	rs104893760
ensembl	rs104893760
geneview	rs104893760
scholar	rs104893760
google	rs104893760
pharmgkb	rs104893760
gwascentral	rs104893760
openSNP	rs104893760
23andMe	rs104893760
SNPshot	rs104893760
SNPdbe	rs104893760
MSV3d	rs104893760
GWAS Ctlg	rs104893760

Max Magnitude

0

OMIM	173110
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104893760(T;T)
Alt	rs104893760(T;T)
Reference	Rs104893760(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.87309172C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000014577.25,