SNP information rs3814995
Normal allele: CC
The nephrin gene (NPHS1) is associated with congenital steroid-resistant nephrotic syndrome.
Polymorphism rs3814995 is related to topics like this:
The most prevalent type of PKD is Autosomal dominant polycystic kidney disease (ADPKD). This...
Research and publications:
15086927 Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).
16316524 [NPHS1 mutations in a Chinese family with congenital nephrotic syndrome].
23349334 Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.
24350232 Multiple hypotheses testing procedures in clinical trials and genomic studies.
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