List of variants in gene combination KIRREL2, NPHS1 reported as benign for Finnish congenital nephrotic syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_004646.4(NPHS1):c.-81C>G	rs73928331	0.07300
NM_004646.4(NPHS1):c.59-5C>G	rs114595892	0.01945
NM_004646.4(NPHS1):c.43G>C (p.Gly15Arg)	rs73928330	0.00456
NM_004646.4(NPHS1):c.59-19C>A	rs115350784	0.00214
NM_004646.4(NPHS1):c.151C>T (p.Leu51=)	rs114385015	0.00057
NM_004646.4(NPHS1):c.65C>T (p.Ala22Val)	rs116617171	0.00023
NM_004646.4(NPHS1):c.-489GA[10]	rs139954720

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