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rs1057517022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517022(-;-)
Make rs1057517022(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position35844419
GeneNPHS1
is asnp
is mentioned by
dbSNPrs1057517022
dbSNP (old)rs1057517022
ClinGenrs1057517022
ebirs1057517022
HLIrs1057517022
Exacrs1057517022
Gnomadrs1057517022
Varsomers1057517022
Maprs1057517022
PheGenIrs1057517022
Biobankrs1057517022
1000 genomesrs1057517022
hgdprs1057517022
ensemblrs1057517022
gopubmedrs1057517022
geneviewrs1057517022
scholarrs1057517022
googlers1057517022
pharmgkbrs1057517022
gwascentralrs1057517022
openSNPrs1057517022
23andMers1057517022
23andMe allrs1057517022
SNPshotrs1057517022
SNPdbers1057517022
MSV3drs1057517022
GWAS Ctlgrs1057517022
Max Magnitude0
ClinVar
Risk rs1057517022(-;-)
Alt rs1057517022(-;-)
Reference Rs1057517022(C;C)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36335321delG
CLNSRC
CLNACC RCV000410557.1,