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rs730880176

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880176(A;A)
Make rs730880176(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position35831147
GeneNPHS1
is asnp
is mentioned by
dbSNPrs730880176
ebirs730880176
HLIrs730880176
Exacrs730880176
Varsomers730880176
Maprs730880176
PheGenIrs730880176
hapmaprs730880176
1000 genomesrs730880176
hgdprs730880176
ensemblrs730880176
gopubmedrs730880176
geneviewrs730880176
scholarrs730880176
googlers730880176
pharmgkbrs730880176
gwascentralrs730880176
openSNPrs730880176
23andMers730880176
23andMe allrs730880176
SNP Nexus

SNPshotrs730880176
SNPdbers730880176
MSV3drs730880176
GWAS Ctlgrs730880176
Max Magnitude0
ClinVar
Risk rs730880176(A;A)
Alt rs730880176(A;A)
Reference rs730880176(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.36322049C>T
CLNSRC
CLNACC RCV000157403.1,