rs587776683

Orientation

plus

Stabilized

plus

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

Make rs587776683(-;-)

Make rs587776683(-;T)

Reference

GRCh38 38.1/142

Chromosome

5

Position

177994298

Gene

PROP1

is a	snp
is	mentioned by
dbSNP	rs587776683
dbSNP (classic)	rs587776683
ClinGen	rs587776683
ebi	rs587776683
HLI	rs587776683
Exac	rs587776683
Gnomad	rs587776683
Varsome	rs587776683
LitVar	rs587776683
Map	rs587776683
PheGenI	rs587776683
Biobank	rs587776683
1000 genomes	rs587776683
hgdp	rs587776683
ensembl	rs587776683
geneview	rs587776683
scholar	rs587776683
google	rs587776683
pharmgkb	rs587776683
gwascentral	rs587776683
openSNP	rs587776683
23andMe	rs587776683
SNPshot	rs587776683
SNPdbe	rs587776683
MSV3d	rs587776683
GWAS Ctlg	rs587776683

Max Magnitude

0

ClinVar
Risk	rs587776683(-;-)
Alt	rs587776683(-;-)
Reference	Rs587776683(T;T)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	PROP1
CLNDBN	Pituitary hormone deficiency, combined 2
Reversed	0
HGVS	NC_000005.9:g.177421299delT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008570.4,