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rs758498695

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs758498695(C;T)
Make rs758498695(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position132713256
GeneNPHP3, NPHP3-ACAD11
is asnp
is mentioned by
dbSNPrs758498695
ebirs758498695
HLIrs758498695
Exacrs758498695
Varsomers758498695
Maprs758498695
PheGenIrs758498695
hapmaprs758498695
1000 genomesrs758498695
hgdprs758498695
ensemblrs758498695
gopubmedrs758498695
geneviewrs758498695
scholarrs758498695
googlers758498695
pharmgkbrs758498695
gwascentralrs758498695
openSNPrs758498695
23andMers758498695
23andMe allrs758498695
SNP Nexus

SNPshotrs758498695
SNPdbers758498695
MSV3drs758498695
GWAS Ctlgrs758498695
Max Magnitude0
ClinVar
Risk rs758498695(T;T)
Alt rs758498695(T;T)
Reference rs758498695(C;C)
Significance Probable-Pathogenic
Disease Nephronophthisis
Variation info
Gene NPHP3 NPHP3-ACAD11
CLNDBN Nephronophthisis
Reversed 0
HGVS NC_000003.11:g.132432100C>T
CLNSRC
CLNACC RCV000197404.1,