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rs386833873(-;CT)

From SNPedia
Carrier of a Finnish congenital nephrotic syndrome (NPHS1) mutation
Is agenotype
ofrs386833873
GeneNPHS1, KIRREL2
Chromosome19
Position35,851,609
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(-;CT) 3 Carrier of a Finnish congenital nephrotic syndrome (NPHS1) mutation
(CT;CT) 0 common in clinvar

Unaffected in absence of a second NPHS1 gene mutation