rs766256429

Orientation

plus

Stabilized

plus

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

Make rs766256429(C;G)

Make rs766256429(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

35806474

Gene

NPR2

is a	snp
is	mentioned by
dbSNP	rs766256429
dbSNP (classic)	rs766256429
ClinGen	rs766256429
ebi	rs766256429
HLI	rs766256429
Exac	rs766256429
Gnomad	rs766256429
Varsome	rs766256429
LitVar	rs766256429
Map	rs766256429
PheGenI	rs766256429
Biobank	rs766256429
1000 genomes	rs766256429
hgdp	rs766256429
ensembl	rs766256429
geneview	rs766256429
scholar	rs766256429
google	rs766256429
pharmgkb	rs766256429
gwascentral	rs766256429
openSNP	rs766256429
23andMe	rs766256429
SNPshot	rs766256429
SNPdbe	rs766256429
MSV3d	rs766256429
GWAS Ctlg	rs766256429

Max Magnitude

0

ClinVar
Risk	rs766256429(G;G) rs766256429(T;T)
Alt	rs766256429(G;G) rs766256429(T;T)
Reference	Rs766256429(C;C)
Significance	Pathogenic
Disease	Short stature with nonspecific skeletal abnormalities
Variation	info
Gene	NPR2
CLNDBN	Short stature with nonspecific skeletal abnormalities
Reversed	0
HGVS	NC_000009.11:g.35806471C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000190428.3,