rs121909361

Orientation

plus

Stabilized

plus

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

Make rs121909361(A;A)

Make rs121909361(A;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

42688937

Gene

GHR

is a	snp
is	mentioned by
dbSNP	rs121909361
dbSNP (classic)	rs121909361
ClinGen	rs121909361
ebi	rs121909361
HLI	rs121909361
Exac	rs121909361
Gnomad	rs121909361
Varsome	rs121909361
LitVar	rs121909361
Map	rs121909361
PheGenI	rs121909361
Biobank	rs121909361
1000 genomes	rs121909361
hgdp	rs121909361
ensembl	rs121909361
geneview	rs121909361
scholar	rs121909361
google	rs121909361
pharmgkb	rs121909361
gwascentral	rs121909361
openSNP	rs121909361
23andMe	rs121909361
SNPshot	rs121909361
SNPdbe	rs121909361
MSV3d	rs121909361
GWAS Ctlg	rs121909361

Max Magnitude

0

OMIM	600946
Desc
Variant	0006
Related	also

ClinVar
Risk	rs121909361(A;A)
Alt	rs121909361(A;A)
Reference	Rs121909361(G;G)
Significance	Pathogenic
Disease	Short stature
Variation	info
Gene	GHR
CLNDBN	Short stature, idiopathic, autosomal
Reversed	0
HGVS	NC_000005.9:g.42689039G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009168.4,