List of variants in gene RAD50 reported as uncertain significance by GeneKor MSA

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_005732.4(RAD50):c.3036+5G>A	rs181016343	0.00078
NM_005732.4(RAD50):c.1094G>A (p.Arg365Gln)	rs146370443	0.00026
NM_005732.4(RAD50):c.2288G>A (p.Arg763His)	rs141989813	0.00026
NM_005732.4(RAD50):c.2177G>A (p.Arg726His)	rs28903092	0.00025
NM_005732.4(RAD50):c.1277A>G (p.Gln426Arg)	rs145428112	0.00015
NM_005732.4(RAD50):c.1663A>G (p.Ile555Val)	rs201120953	0.00006
NM_005732.4(RAD50):c.281T>C (p.Ile94Thr)	rs768127412	0.00004
NM_005732.4(RAD50):c.695C>A (p.Ala232Asp)	rs28903089	0.00004
NM_005732.4(RAD50):c.785T>G (p.Leu262Arg)	rs201728859	0.00003
NM_005732.4(RAD50):c.1604G>A (p.Arg535His)	rs200548021	0.00002
NM_005732.4(RAD50):c.2492A>G (p.Glu831Gly)	rs772155267	0.00001
NM_005732.4(RAD50):c.578G>A (p.Arg193Gln)	rs776046799	0.00001
NM_005732.4(RAD50):c.1429C>A (p.Leu477Met)	rs1211437074
NM_005732.4(RAD50):c.1680T>G (p.Ser560Arg)	rs786203901
NM_005732.4(RAD50):c.2604T>G (p.Asn868Lys)	rs786202498
NM_005732.4(RAD50):c.34G>C (p.Val12Leu)	rs755022536
NM_005732.4(RAD50):c.587G>A (p.Arg196His)	rs764784659

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