List of variants in gene MRE11 reported as likely pathogenic 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_005591.4(MRE11):c.1015A>T (p.Lys339Ter)	rs984874083	0.00004
NM_005591.4(MRE11):c.545-1G>A	rs1451215042	0.00002
NM_005591.4(MRE11):c.77T>C (p.Met26Thr)	rs372068015	0.00002
NM_005591.4(MRE11):c.315-2A>G	rs876659145	0.00001
NM_005591.4(MRE11):c.350A>G (p.Asn117Ser)	rs137852760	0.00001
NM_005591.4(MRE11):c.1047_1048del (p.Glu350fs)	rs1591688367
NM_005591.4(MRE11):c.1222dup (p.Thr408fs)	rs774440500
NM_005591.4(MRE11):c.1742_1743insAT (p.Gln582fs)
NM_005591.4(MRE11):c.295_298del (p.Val99fs)	rs1555017184
NM_005591.4(MRE11):c.314+2T>C	rs1591718826
NM_005591.4(MRE11):c.821_823delinsA (p.Leu274fs)	rs786202032
NM_005591.4(MRE11):c.845+6T>G	rs2135045937
NM_005591.4(MRE11):c.939del (p.Val313_Leu314insTer)

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