List of variants in gene PRDM16 reported as likely benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.100G>A (p.Ala34Thr)	rs187194973	0.00252
NM_022114.4(PRDM16):c.2506G>A (p.Gly836Ser)	rs114204766	0.00168
NM_022114.4(PRDM16):c.2452G>A (p.Gly818Ser)	rs201904226	0.00160
NM_022114.4(PRDM16):c.201G>A (p.Pro67=)	rs199614349	0.00153
NM_022114.4(PRDM16):c.3102C>T (p.Asn1034=)	rs199853370	0.00144
NM_022114.4(PRDM16):c.2290G>A (p.Val764Met)	rs149333409	0.00117
NM_022114.4(PRDM16):c.3621A>T (p.Glu1207Asp)	rs199972068	0.00117
NM_022114.4(PRDM16):c.3154G>A (p.Ala1052Thr)	rs113879347	0.00072
NM_022114.4(PRDM16):c.2634C>T (p.Pro878=)	rs201338158	0.00065
NM_022114.4(PRDM16):c.934G>A (p.Asp312Asn)	rs191798831	0.00060
NM_022114.4(PRDM16):c.1632C>T (p.Asp544=)	rs199499877	0.00034
NM_022114.4(PRDM16):c.2748G>A (p.Ala916=)	rs370768364	0.00015
NM_022114.4(PRDM16):c.1033-10G>A	rs370090853	0.00013
NM_022114.4(PRDM16):c.1668G>A (p.Leu556=)	rs372910329	0.00013
NM_022114.4(PRDM16):c.2503G>A (p.Ala835Thr)	rs755872965	0.00009
NM_022114.4(PRDM16):c.2259C>T (p.Ala753=)	rs548246861	0.00003
NM_022114.4(PRDM16):c.801G>A (p.Glu267=)	rs369972213	0.00002
NM_022114.4(PRDM16):c.3288G>A (p.Ala1096=)	rs754951901	0.00001
NM_022114.4(PRDM16):c.2448C>T (p.Asn816=)	rs372189819
NM_022114.4(PRDM16):c.2468G>C (p.Arg823Pro)	rs371654192

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