List of variants reported as likely benign for Hennekam lymphangiectasia-lymphedema syndrome 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.14361C>T (p.Val4787=)	rs1014865	0.01862
NM_001291303.3(FAT4):c.8592G>A (p.Val2864=)	rs111758803	0.01583
NM_001291303.3(FAT4):c.1101A>G (p.Val367=)	rs57692448	0.01498
NM_001291303.3(FAT4):c.12713C>T (p.Ala4238Val)	rs183396105	0.00087
NM_001291303.3(FAT4):c.5054G>A (p.Arg1685Gln)	rs376422522	0.00034
NM_001291303.3(FAT4):c.3642T>G (p.Phe1214Leu)	rs201264765	0.00033
NM_001291303.3(FAT4):c.4432A>C (p.Ile1478Leu)	rs200565115	0.00033
NM_001291303.3(FAT4):c.8854A>C (p.Ser2952Arg)	rs538489921	0.00029
NM_001291303.3(FAT4):c.5401C>T (p.Arg1801Trp)	rs201887525	0.00013
NM_001291303.3(FAT4):c.14935G>A (p.Ala4979Thr)	rs17009858	0.00011
NM_001291303.3(FAT4):c.10571G>A (p.Arg3524Gln)	rs200082059	0.00006
NM_001291303.3(FAT4):c.9896G>A (p.Arg3299His)	rs370611770	0.00004
NM_001291303.3(FAT4):c.6210C>T (p.Phe2070=)	rs771989829	0.00003
NM_001291303.3(FAT4):c.842C>T (p.Thr281Ile)	rs564305264	0.00001
NM_001291303.3(FAT4):c.7125G>A (p.Glu2375=)

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