rs193922466

Orientation

plus

Stabilized

plus

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

Make rs193922466(A;G)

Make rs193922466(G;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

634687

Gene

SHOX

is a	snp
is	mentioned by
dbSNP	rs193922466
dbSNP (classic)	rs193922466
ClinGen	rs193922466
ebi	rs193922466
HLI	rs193922466
Exac	rs193922466
Gnomad	rs193922466
Varsome	rs193922466
LitVar	rs193922466
Map	rs193922466
PheGenI	rs193922466
Biobank	rs193922466
1000 genomes	rs193922466
hgdp	rs193922466
ensembl	rs193922466
geneview	rs193922466
scholar	rs193922466
google	rs193922466
pharmgkb	rs193922466
gwascentral	rs193922466
openSNP	rs193922466
23andMe	rs193922466
SNPshot	rs193922466
SNPdbe	rs193922466
MSV3d	rs193922466
GWAS Ctlg	rs193922466

Max Magnitude

0

ClinVar
Risk	rs193922466(G;G)
Alt	rs193922466(G;G)
Reference	Rs193922466(A;A)
Significance	Probable-Pathogenic
Disease	Short stature
Variation	info
Gene	SHOX
CLNDBN	Short stature, idiopathic, X-linked
Reversed	0
HGVS	NC_000023.10:g.595422A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030453.1,