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rs786204708

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786204708(A;A)
Make rs786204708(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position179561287
GeneNPHS2
is asnp
is mentioned by
dbSNPrs786204708
ebirs786204708
HLIrs786204708
Exacrs786204708
Varsomers786204708
Maprs786204708
PheGenIrs786204708
hapmaprs786204708
1000 genomesrs786204708
hgdprs786204708
ensemblrs786204708
gopubmedrs786204708
geneviewrs786204708
scholarrs786204708
googlers786204708
pharmgkbrs786204708
gwascentralrs786204708
openSNPrs786204708
23andMers786204708
23andMe allrs786204708
SNP Nexus

SNPshotrs786204708
SNPdbers786204708
MSV3drs786204708
GWAS Ctlgrs786204708
Max Magnitude0
ClinVar
Risk rs786204708(A;A)
Alt rs786204708(A;A)
Reference rs786204708(T;T)
Significance Probable-Pathogenic
Disease Nephrotic syndrome
Variation info
Gene NPHS2
CLNDBN Nephrotic syndrome, idiopathic, steroid-resistant
Reversed 1
HGVS NC_000001.10:g.179530422A>T
CLNSRC Counsyl
CLNACC RCV000169523.1,