List of variants reported as likely benign for Seckel syndrome 1; Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.6339A>G (p.Val2113=)	rs7635479	0.00964
NM_001184.4(ATR):c.7504-16A>G	rs111927479	0.00279
NM_001184.4(ATR):c.7902C>T (p.Cys2634=)	rs553715098	0.00008
NM_001184.4(ATR):c.7192+19A>G	rs376334522	0.00005

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