rs587776662

Orientation

plus

Stabilized

plus

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

Make rs587776662(-;C)

Make rs587776662(C;C)

Reference

GRCh38 38.1/142

Chromosome

1

Position

180266436

Gene

LHX4

is a	snp
is	mentioned by
dbSNP	rs587776662
dbSNP (classic)	rs587776662
ClinGen	rs587776662
ebi	rs587776662
HLI	rs587776662
Exac	rs587776662
Gnomad	rs587776662
Varsome	rs587776662
LitVar	rs587776662
Map	rs587776662
PheGenI	rs587776662
Biobank	rs587776662
1000 genomes	rs587776662
hgdp	rs587776662
ensembl	rs587776662
geneview	rs587776662
scholar	rs587776662
google	rs587776662
pharmgkb	rs587776662
gwascentral	rs587776662
openSNP	rs587776662
23andMe	rs587776662
SNPshot	rs587776662
SNPdbe	rs587776662
MSV3d	rs587776662
GWAS Ctlg	rs587776662

Max Magnitude

0

ClinVar
Risk	rs587776662(C;C)
Alt	rs587776662(C;C)
Reference	Rs587776662(-;-)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	LHX4
CLNDBN	Pituitary hormone deficiency, combined 4
Reversed	0
HGVS	NC_000001.10:g.180235571dupC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007940.3,