Have questions? Visit https://www.reddit.com/r/SNPedia

rs771373457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771373457(G;T)
Make rs771373457(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position35808833
GeneNPR2, SPAG8
is asnp
is mentioned by
dbSNPrs771373457
dbSNP (old)rs771373457
ClinGenrs771373457
ebirs771373457
HLIrs771373457
Exacrs771373457
Gnomadrs771373457
Varsomers771373457
LitVarrs771373457
Maprs771373457
PheGenIrs771373457
Biobankrs771373457
1000 genomesrs771373457
hgdprs771373457
ensemblrs771373457
gopubmedrs771373457
geneviewrs771373457
scholarrs771373457
googlers771373457
pharmgkbrs771373457
gwascentralrs771373457
openSNPrs771373457
23andMers771373457
23andMe allrs771373457
SNPshotrs771373457
SNPdbers771373457
MSV3drs771373457
GWAS Ctlgrs771373457
Max Magnitude0
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,