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rs1085307906

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position35800397
GeneNPR2
is asnp
is mentioned by
dbSNPrs1085307906
dbSNP (old)rs1085307906
ClinGenrs1085307906
ebirs1085307906
HLIrs1085307906
Exacrs1085307906
Gnomadrs1085307906
Varsomers1085307906
Maprs1085307906
PheGenIrs1085307906
Biobankrs1085307906
1000 genomesrs1085307906
hgdprs1085307906
ensemblrs1085307906
gopubmedrs1085307906
geneviewrs1085307906
scholarrs1085307906
googlers1085307906
pharmgkbrs1085307906
gwascentralrs1085307906
openSNPrs1085307906
23andMers1085307906
23andMe allrs1085307906
SNPshotrs1085307906
SNPdbers1085307906
MSV3drs1085307906
GWAS Ctlgrs1085307906
Max Magnitude0
ClinVar
Risk rs1085307906(A;A)
Alt rs1085307906(A;A)
Reference Rs1085307906(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPR2
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.35800394G>A
CLNSRC
CLNACC RCV000489591.1,