List of variants in gene MED25 reported as benign by Invitae

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.165G>A (p.Thr55=)	rs77400039	0.01828
NM_030973.4(MED25):c.1483-7C>T	rs2017698	0.01612
NM_030973.4(MED25):c.2031G>A (p.Ala677=)	rs57854058	0.01517
NM_030973.4(MED25):c.1727C>G (p.Ala576Gly)	rs193291405	0.00836
NM_030973.4(MED25):c.1482+19G>A	rs4802632	0.00704
NM_030973.4(MED25):c.2056C>T (p.Leu686=)	rs201969940	0.00598
NM_030973.4(MED25):c.1794C>T (p.Ala598=)	rs185100172	0.00456
NM_030973.4(MED25):c.93C>T (p.Tyr31=)	rs61742955	0.00394
NM_030973.4(MED25):c.2088G>A (p.Leu696=)	rs371157406	0.00252
NM_030973.4(MED25):c.688+17G>A	rs373952366	0.00188
NM_030973.4(MED25):c.819+14C>T	rs188257265	0.00166
NM_030973.4(MED25):c.396C>T (p.Arg132=)	rs142353864	0.00125
NM_030973.4(MED25):c.1675-7C>T	rs79635160	0.00123
NM_030973.4(MED25):c.1374+9C>T	rs574703435	0.00090
NM_030973.4(MED25):c.2208C>T (p.Ser736=)	rs376796439	0.00030
NM_030973.4(MED25):c.1434G>A (p.Lys478=)	rs181389801	0.00028
NM_030973.4(MED25):c.1062C>T (p.Ser354=)	rs140345077	0.00026
NM_030973.4(MED25):c.404+16A>G	rs190980102	0.00026
NM_030973.4(MED25):c.96C>T (p.Phe32=)	rs138246339	0.00003
NM_030973.4(MED25):c.1143A>G (p.Pro381=)	rs200571306	0.00001
NM_030973.4(MED25):c.1101+24_1101+42dup	rs564179307
NM_030973.4(MED25):c.1231-5dup	rs778157941
NM_030973.4(MED25):c.1369C>T (p.Leu457=)	rs566536708
NM_030973.4(MED25):c.1482+21dup
NM_030973.4(MED25):c.1674+19C>T	rs752522
NM_030973.4(MED25):c.2146+19G>T	rs568964675
NM_030973.4(MED25):c.2146+8del
NM_030973.4(MED25):c.234C>G (p.Pro78=)	rs74863643
NM_030973.4(MED25):c.525+20_525+34del	rs766617168
NM_030973.4(MED25):c.597C>A (p.Ala199=)	rs149788020

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