RS115308424 NPHS1

Health Risk Chr 19:35849272 snv missense variant
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Associated Conditions
Congenital nephrotic syndrome
Finnish congenital nephrotic syndrome
Focal segmental glomerulosclerosis
Congenital nephrotic syndrome
Finnish congenital nephrotic syndrome
Focal segmental glomerulosclerosis
Population Frequencies
gnomAD ALL
0%
1kG AFR
0.1%
1kG ALL
0.6%
1kG AMR
100%
1kG EAS
98%
1kG EUR
100%
1kG SAS
99.2%
Other Variants in NPHS1
rs1973075631 rs1972884983 rs1972875644 rs2527606158 rs28939695 rs267606919 rs267606917 rs267606918 rs139954720 rs386833862
Ask Dr. Hemsworth about this variant