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rs869312915

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312915(G;G)
Make rs869312915(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position132699418
GeneNPHP3, NPHP3-ACAD11
is asnp
is mentioned by
dbSNPrs869312915
ebirs869312915
HLIrs869312915
Exacrs869312915
Varsomers869312915
Maprs869312915
PheGenIrs869312915
hapmaprs869312915
1000 genomesrs869312915
hgdprs869312915
ensemblrs869312915
gopubmedrs869312915
geneviewrs869312915
scholarrs869312915
googlers869312915
pharmgkbrs869312915
gwascentralrs869312915
openSNPrs869312915
23andMers869312915
23andMe allrs869312915
SNP Nexus

SNPshotrs869312915
SNPdbers869312915
MSV3drs869312915
GWAS Ctlgrs869312915
Max Magnitude0
ClinVar
Risk rs869312915(G;G)
Alt rs869312915(G;G)
Reference rs869312915(T;T)
Significance Probable-Pathogenic
Disease Inborn genetic diseases
Variation info
Gene NPHP3 NPHP3-ACAD11
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000003.11:g.132418262A>C
CLNSRC
CLNACC RCV000210561.1,