List of variants in gene MED25 reported as likely benign for not provided

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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: 25

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.1375-58A>G	rs3745479	0.02762
NM_030973.4(MED25):c.689-27G>C	rs112946131	0.01303
NM_030973.4(MED25):c.525+28G>A	rs183713569	0.00874
NM_030973.4(MED25):c.1004C>T (p.Ala335Val)	rs145770066	0.00443
NM_030973.4(MED25):c.2088G>A (p.Leu696=)	rs371157406	0.00252
NM_030973.4(MED25):c.396C>T (p.Arg132=)	rs142353864	0.00125
NM_030973.4(MED25):c.354C>T (p.Leu118=)	rs145574885	0.00110
NM_030973.4(MED25):c.135-6T>G	rs199743509	0.00036
NM_030973.4(MED25):c.1095G>A (p.Pro365=)	rs373128874	0.00017
NM_030973.4(MED25):c.942C>T (p.Pro314=)	rs373971747	0.00009
NM_030973.4(MED25):c.1038G>T (p.Leu346=)	rs759964732	0.00006
NM_030973.4(MED25):c.1572C>T (p.Gly524=)	rs559482732	0.00005
NM_030973.4(MED25):c.1335C>T (p.Pro445=)	rs372191174	0.00004
NM_030973.4(MED25):c.678C>T (p.Leu226=)	rs770604129	0.00003
NM_030973.4(MED25):c.384C>T (p.Phe128=)	rs1204577575	0.00001
NM_030973.4(MED25):c.954C>T (p.Pro318=)	rs554447029	0.00001
NM_030973.4(MED25):c.1275G>A (p.Arg425=)
NM_030973.4(MED25):c.150T>G (p.Gly50=)	rs1600311781
NM_030973.4(MED25):c.1788A>G (p.Val596=)
NM_030973.4(MED25):c.1887C>T (p.Pro629=)
NM_030973.4(MED25):c.228C>T (p.Cys76=)	rs770196362
NM_030973.4(MED25):c.633A>G (p.Thr211=)	rs369117035
NM_030973.4(MED25):c.654G>A (p.Arg218=)	rs1600324452
NM_030973.4(MED25):c.735C>T (p.Val245=)
NM_030973.4(MED25):c.908-6C>A

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