rs757744435

Orientation

plus

Stabilized

plus

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

Make rs757744435(A;T)

Make rs757744435(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

35794009

Gene

NPR2

is a	snp
is	mentioned by
dbSNP	rs757744435
dbSNP (classic)	rs757744435
ClinGen	rs757744435
ebi	rs757744435
HLI	rs757744435
Exac	rs757744435
Gnomad	rs757744435
Varsome	rs757744435
LitVar	rs757744435
Map	rs757744435
PheGenI	rs757744435
Biobank	rs757744435
1000 genomes	rs757744435
hgdp	rs757744435
ensembl	rs757744435
geneview	rs757744435
scholar	rs757744435
google	rs757744435
pharmgkb	rs757744435
gwascentral	rs757744435
openSNP	rs757744435
23andMe	rs757744435
SNPshot	rs757744435
SNPdbe	rs757744435
MSV3d	rs757744435
GWAS Ctlg	rs757744435

Max Magnitude

0

ClinVar
Risk	rs757744435(G;G) rs757744435(T;T)
Alt	rs757744435(G;G) rs757744435(T;T)
Reference	Rs757744435(A;A)
Significance	Probable-Pathogenic
Disease	Craniosynostosis Growth delay Limb undergrowth Trident hand
Variation	info
Gene	NPR2
CLNDBN	Craniosynostosis Growth delay Limb undergrowth Trident hand
Reversed	0
HGVS	NC_000009.11:g.35794006A>T
CLNSRC
CLNACC	RCV000414841.1,