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rs386833935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386833935(-;-)
Make rs386833935(-;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35831679
GeneNPHS1
is asnp
is mentioned by
dbSNPrs386833935
ebirs386833935
HLIrs386833935
Exacrs386833935
Varsomers386833935
Maprs386833935
PheGenIrs386833935
hapmaprs386833935
1000 genomesrs386833935
hgdprs386833935
ensemblrs386833935
gopubmedrs386833935
geneviewrs386833935
scholarrs386833935
googlers386833935
pharmgkbrs386833935
gwascentralrs386833935
openSNPrs386833935
23andMers386833935
23andMe allrs386833935
SNP Nexus

SNPshotrs386833935
SNPdbers386833935
MSV3drs386833935
GWAS Ctlgrs386833935
Max Magnitude0
ClinVar
Risk rs386833935(;)
Alt rs386833935(;)
Reference rs386833935(G;G)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36322581delC
CLNSRC ClinVar
CLNACC RCV000049909.1,


[PMID 10577936OA-icon.png] Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the old order Mennonites.