List of variants in gene FAM161A reported as benign for Retinitis pigmentosa 28

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

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_032180.2(FAM161A):c.-41T>C	rs1881616	0.98184
NM_001201543.2(FAM161A):c.1212T>C (p.Cys404=)	rs4672457	0.98181
NM_001201543.2(FAM161A):c.184-33G>A	rs11125896	0.20547
NM_001201543.2(FAM161A):c.1584-11G>A	rs17513666	0.17214
NM_001201543.2(FAM161A):c.706A>G (p.Ile236Val)	rs17513722	0.17102
NM_001201543.2(FAM161A):c.321A>G (p.Ile107Met)	rs11125895	0.16195
NM_001201543.2(FAM161A):c.1665G>A (p.Leu555=)	rs6545910	0.10308
NM_001201543.2(FAM161A):c.817G>A (p.Glu273Lys)	rs6733774	0.00570
NM_001201543.2(FAM161A):c.197C>T (p.Thr66Ile)	rs145199539	0.00372
NM_001201543.2(FAM161A):c.1959G>T (p.Glu653Asp)	rs201052209	0.00010

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