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rs369162678

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs369162678(A;A)
Make rs369162678(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position5863955
GeneMIR4689, NPHP4
is asnp
is mentioned by
dbSNPrs369162678
ebirs369162678
HLIrs369162678
Exacrs369162678
Varsomers369162678
Maprs369162678
PheGenIrs369162678
hapmaprs369162678
1000 genomesrs369162678
hgdprs369162678
ensemblrs369162678
gopubmedrs369162678
geneviewrs369162678
scholarrs369162678
googlers369162678
pharmgkbrs369162678
gwascentralrs369162678
openSNPrs369162678
23andMers369162678
23andMe allrs369162678
SNP Nexus

SNPshotrs369162678
SNPdbers369162678
MSV3drs369162678
GWAS Ctlgrs369162678
Max Magnitude0
ClinVar
Risk rs369162678(A;A)
Alt rs369162678(A;A)
Reference rs369162678(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPHP4 MIR4689
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.5924015G>A
CLNSRC
CLNACC RCV000171146.1,