rs137854506

Orientation

minus

Stabilized

minus

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

Make rs137854506(A;T)

Make rs137854506(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

136200700

Gene

LHX3

is a	snp
is	mentioned by
dbSNP	rs137854506
dbSNP (classic)	rs137854506
ClinGen	rs137854506
ebi	rs137854506
HLI	rs137854506
Exac	rs137854506
Gnomad	rs137854506
Varsome	rs137854506
LitVar	rs137854506
Map	rs137854506
PheGenI	rs137854506
Biobank	rs137854506
1000 genomes	rs137854506
hgdp	rs137854506
ensembl	rs137854506
geneview	rs137854506
scholar	rs137854506
google	rs137854506
pharmgkb	rs137854506
gwascentral	rs137854506
openSNP	rs137854506
23andMe	rs137854506
SNPshot	rs137854506
SNPdbe	rs137854506
MSV3d	rs137854506
GWAS Ctlg	rs137854506

Max Magnitude

0

OMIM	600577
Desc
Variant	0009
Related	also

ClinVar
Risk	rs137854506(T;T)
Alt	rs137854506(T;T)
Reference	Rs137854506(A;A)
Significance	Pathogenic
Disease	Pituitary hormone deficiency
Variation	info
Gene	LHX3
CLNDBN	Pituitary hormone deficiency, combined 3
Reversed	1
HGVS	NC_000009.11:g.139092546T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009595.2,