List of variants in gene POR reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001395413.1(POR):c.1707G>A (p.Ser569=)	rs1057870	0.28425
NM_001395413.1(POR):c.1499C>T (p.Ala500Val)	rs1057868	0.26722
NM_001395413.1(POR):c.6A>G (p.Gly2=)	rs10262966	0.07713
NM_001395413.1(POR):c.360C>T (p.Ala120=)	rs41299490	0.00719
NM_001395413.1(POR):c.78G>A (p.Thr26=)	rs41295381	0.00681
NM_001395413.1(POR):c.1889+3G>A	rs41301439	0.00568
NM_001395413.1(POR):c.508-4G>A	rs41299496	0.00462
NM_001395413.1(POR):c.508-14_508-13del	rs72557912	0.00363
NM_001395413.1(POR):c.1227C>T (p.Ser409=)	rs41301424	0.00041

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