List of variants reported as likely pathogenic for retinitis pigmentosa 37 by Fulgent Genetics, Fulgent Genetics

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_014249.4(NR2E3):c.646G>A (p.Gly216Ser)	rs368098126	0.00006
NM_014249.4(NR2E3):c.229C>T (p.Arg77Trp)	rs779903522	0.00003
NM_014249.4(NR2E3):c.305C>A (p.Ala102Asp)	rs772881093	0.00003
NM_014249.4(NR2E3):c.364C>T (p.Arg122Cys)	rs527236086	0.00002
NM_014249.4(NR2E3):c.1049A>G (p.Gln350Arg)
NM_014249.4(NR2E3):c.1112T>G (p.Leu371Trp)
NM_014249.4(NR2E3):c.16_47del (p.Thr6fs)
NM_014249.4(NR2E3):c.242A>G (p.Tyr81Cys)
NM_014249.4(NR2E3):c.263G>T (p.Gly88Val)	rs1278137915
NM_014249.4(NR2E3):c.302_325del (p.Gln101_Cys108del)
NM_014249.4(NR2E3):c.532dup (p.Ile178fs)

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