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rs730880174

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880174(A;G)
Make rs730880174(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position35845670
GeneNPHS1
is asnp
is mentioned by
dbSNPrs730880174
ebirs730880174
HLIrs730880174
Exacrs730880174
Varsomers730880174
Maprs730880174
PheGenIrs730880174
hapmaprs730880174
1000 genomesrs730880174
hgdprs730880174
ensemblrs730880174
gopubmedrs730880174
geneviewrs730880174
scholarrs730880174
googlers730880174
pharmgkbrs730880174
gwascentralrs730880174
openSNPrs730880174
23andMers730880174
23andMe allrs730880174
SNP Nexus

SNPshotrs730880174
SNPdbers730880174
MSV3drs730880174
GWAS Ctlgrs730880174
Max Magnitude0
ClinVar
Risk rs730880174(G;G)
Alt rs730880174(G;G)
Reference rs730880174(A;A)
Significance Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36336572T>C
CLNSRC
CLNACC RCV000157399.1,