Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057516637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057516637(-;C)
Make rs1057516637(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position35835755
GeneNPHS1
is asnp
is mentioned by
dbSNPrs1057516637
dbSNP (old)rs1057516637
ClinGenrs1057516637
ebirs1057516637
HLIrs1057516637
Exacrs1057516637
Gnomadrs1057516637
Varsomers1057516637
Maprs1057516637
PheGenIrs1057516637
Biobankrs1057516637
1000 genomesrs1057516637
hgdprs1057516637
ensemblrs1057516637
gopubmedrs1057516637
geneviewrs1057516637
scholarrs1057516637
googlers1057516637
pharmgkbrs1057516637
gwascentralrs1057516637
openSNPrs1057516637
23andMers1057516637
23andMe allrs1057516637
SNPshotrs1057516637
SNPdbers1057516637
MSV3drs1057516637
GWAS Ctlgrs1057516637
Max Magnitude0
ClinVar
Risk rs1057516637(C;C)
Alt rs1057516637(C;C)
Reference Rs1057516637(-;-)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36326658dupG
CLNSRC
CLNACC RCV000409058.1,