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rs398123285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398123285(-;-)
Make rs398123285(-;C)
Make rs398123285(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position110160193
GeneNPHP1
is asnp
is mentioned by
dbSNPrs398123285
ebirs398123285
HLIrs398123285
Exacrs398123285
Varsomers398123285
Maprs398123285
PheGenIrs398123285
hapmaprs398123285
1000 genomesrs398123285
hgdprs398123285
ensemblrs398123285
gopubmedrs398123285
geneviewrs398123285
scholarrs398123285
googlers398123285
pharmgkbrs398123285
gwascentralrs398123285
openSNPrs398123285
23andMers398123285
23andMe allrs398123285
SNP Nexus

SNPshotrs398123285
SNPdbers398123285
MSV3drs398123285
GWAS Ctlgrs398123285
Max Magnitude0
ClinVar
Risk rs398123285(C;C)
Alt rs398123285(C;C)
Reference rs398123285(;)
Significance Pathogenic
Disease not provided
Variation info
Gene NPHP1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.110917771dupG
CLNSRC ClinVar
CLNACC RCV000078487.3,