List of variants in gene PTPRO studied for Nephrotic syndrome, type 6

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_030667.3(PTPRO):c.508+19G>A	rs138770041	0.01959
NM_030667.3(PTPRO):c.1110C>G (p.Asn370Lys)	rs61754411	0.01921
NM_030667.3(PTPRO):c.2841G>A (p.Leu947=)	rs61754412	0.00554
NM_030667.3(PTPRO):c.2406T>C (p.Ser802=)	rs61741744	0.00293
NM_030667.3(PTPRO):c.661+9C>T	rs191278870	0.00027
NM_030667.3(PTPRO):c.1611G>T (p.Met537Ile)	rs141255287	0.00022
NM_030667.3(PTPRO):c.1776C>T (p.Ser592=)	rs369419924	0.00001
NM_030667.3(PTPRO):c.497T>C (p.Met166Thr)	rs376857700	0.00001
NM_030667.3(PTPRO):c.1733C>T (p.Thr578Ile)	rs1942611245
NM_030667.3(PTPRO):c.1792C>G (p.Leu598Val)	rs746574149
NM_030667.3(PTPRO):c.2627+1G>T	rs1591732280
NM_030667.3(PTPRO):c.2750C>T (p.Pro917Leu)
NM_030667.3(PTPRO):c.2829+1G>A	rs1591750243
NM_030667.3(PTPRO):c.2920T>C (p.Tyr974His)
NM_030667.3(PTPRO):c.2997+18del	rs751345733
NM_030667.3(PTPRO):c.3222C>T (p.Asp1074=)	rs144347297
NM_030667.3(PTPRO):c.3497G>C (p.Gly1166Ala)	rs528784695
NM_030667.3(PTPRO):c.612C>T (p.Thr204=)	rs139561990

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