List of variants reported as uncertain significance for brittle cornea syndrome 2 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_018699.4(PRDM5):c.248G>A (p.Arg83His)	rs201945549	0.00012
NM_018699.4(PRDM5):c.740C>T (p.Ser247Leu)	rs187637689	0.00006
NM_018699.4(PRDM5):c.93+7G>A	rs777981327	0.00001
NM_018699.4(PRDM5):c.337A>G (p.Ile113Val)
NM_018699.4(PRDM5):c.644A>G (p.Gln215Arg)

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