rs796065355

Orientation

plus

Stabilized

plus

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

Make rs796065355(C;C)

Make rs796065355(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

35792634

Gene

NPR2

is a	snp
is	mentioned by
dbSNP	rs796065355
dbSNP (classic)	rs796065355
ClinGen	rs796065355
ebi	rs796065355
HLI	rs796065355
Exac	rs796065355
Gnomad	rs796065355
Varsome	rs796065355
LitVar	rs796065355
Map	rs796065355
PheGenI	rs796065355
Biobank	rs796065355
1000 genomes	rs796065355
hgdp	rs796065355
ensembl	rs796065355
geneview	rs796065355
scholar	rs796065355
google	rs796065355
pharmgkb	rs796065355
gwascentral	rs796065355
openSNP	rs796065355
23andMe	rs796065355
SNPshot	rs796065355
SNPdbe	rs796065355
MSV3d	rs796065355
GWAS Ctlg	rs796065355

Max Magnitude

0

ClinVar
Risk	rs796065355(C;C)
Alt	rs796065355(C;C)
Reference	Rs796065355(T;T)
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.35792631T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000190429.2,