rs587776712

Orientation

plus

Stabilized

plus

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

Make rs587776712(-;-)

Make rs587776712(-;A)

Reference

GRCh38 38.1/142

Chromosome

9

Position

136200737

Gene

LHX3

is a	snp
is	mentioned by
dbSNP	rs587776712
dbSNP (classic)	rs587776712
ClinGen	rs587776712
ebi	rs587776712
HLI	rs587776712
Exac	rs587776712
Gnomad	rs587776712
Varsome	rs587776712
LitVar	rs587776712
Map	rs587776712
PheGenI	rs587776712
Biobank	rs587776712
1000 genomes	rs587776712
hgdp	rs587776712
ensembl	rs587776712
geneview	rs587776712
scholar	rs587776712
google	rs587776712
pharmgkb	rs587776712
gwascentral	rs587776712
openSNP	rs587776712
23andMe	rs587776712
SNPshot	rs587776712
SNPdbe	rs587776712
MSV3d	rs587776712
GWAS Ctlg	rs587776712

Max Magnitude

0

ClinVar
Risk	rs587776712(-;-)
Alt	rs587776712(-;-)
Reference	Rs587776712(A;A)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	LHX3
CLNDBN	Pituitary hormone deficiency, combined 3
Reversed	0
HGVS	NC_000009.11:g.139092583delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009589.3,