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rs1057517021

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517021(-;-)
Make rs1057517021(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position35845681
GeneNPHS1
is asnp
is mentioned by
dbSNPrs1057517021
dbSNP (old)rs1057517021
ClinGenrs1057517021
ebirs1057517021
HLIrs1057517021
Exacrs1057517021
Gnomadrs1057517021
Varsomers1057517021
LitVarrs1057517021
Maprs1057517021
PheGenIrs1057517021
Biobankrs1057517021
1000 genomesrs1057517021
hgdprs1057517021
ensemblrs1057517021
gopubmedrs1057517021
geneviewrs1057517021
scholarrs1057517021
googlers1057517021
pharmgkbrs1057517021
gwascentralrs1057517021
openSNPrs1057517021
23andMers1057517021
23andMe allrs1057517021
SNPshotrs1057517021
SNPdbers1057517021
MSV3drs1057517021
GWAS Ctlgrs1057517021
Max Magnitude0
ClinVar
Risk rs1057517021(-;-)
Alt rs1057517021(-;-)
Reference Rs1057517021(A;A)
Significance Probable-Pathogenic
Disease Finnish congenital nephrotic syndrome
Variation info
Gene NPHS1
CLNDBN Finnish congenital nephrotic syndrome
Reversed 1
HGVS NC_000019.9:g.36336583delT
CLNSRC
CLNACC RCV000408979.1,