List of variants reported as likely benign for Bloom syndrome by Illumina Laboratory Services, Illumina

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000057.4(BLM):c.4076+4T>G	rs183176301	0.00436
NM_000057.4(BLM):c.2160C>T (p.Ile720=)	rs28385028	0.00303
NM_000057.4(BLM):c.1928G>A (p.Arg643His)	rs12720097	0.00279
NM_000057.4(BLM):c.4077-10C>T	rs145310008	0.00209
NM_000057.4(BLM):c.*77T>A	rs116293756	0.00124
NM_000057.4(BLM):c.11T>C (p.Val4Ala)	rs144706057	0.00104
NM_000057.4(BLM):c.2362C>A (p.Leu788Ile)	rs149754073	0.00086
NM_000057.4(BLM):c.3592G>A (p.Val1198Met)	rs142928725	0.00082
NM_000057.4(BLM):c.2293G>A (p.Val765Ile)	rs191789336	0.00011
NM_000057.4(BLM):c.178T>A (p.Leu60Ile)	rs138542210	0.00007

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