rs771373457

Orientation

plus

Stabilized

plus

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

Make rs771373457(G;T)

Make rs771373457(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

35808833

Gene	NPR2, SPAG8

is a	snp
is	mentioned by
dbSNP	rs771373457
dbSNP (classic)	rs771373457
ClinGen	rs771373457
ebi	rs771373457
HLI	rs771373457
Exac	rs771373457
Gnomad	rs771373457
Varsome	rs771373457
LitVar	rs771373457
Map	rs771373457
PheGenI	rs771373457
Biobank	rs771373457
1000 genomes	rs771373457
hgdp	rs771373457
ensembl	rs771373457
geneview	rs771373457
scholar	rs771373457
google	rs771373457
pharmgkb	rs771373457
gwascentral	rs771373457
openSNP	rs771373457
23andMe	rs771373457
SNPshot	rs771373457
SNPdbe	rs771373457
MSV3d	rs771373457
GWAS Ctlg	rs771373457

Max Magnitude

0

ClinVar
Risk	rs771373457(A;A) rs771373457(T;T)
Alt	rs771373457(A;A) rs771373457(T;T)
Reference	Rs771373457(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NPR2 SPAG8
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.35808830G>T
CLNSRC
CLNACC	RCV000480765.1,