List of variants in gene combination NHP2, RMND5B reported as likely benign for ectodermal dysplasia syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_017838.4(NHP2):c.351C>T (p.Ala117=)	rs115334254	0.01019
NM_017838.4(NHP2):c.337-14T>C	rs201653595	0.00188
NM_017838.4(NHP2):c.369C>T (p.Pro123=)	rs375285426	0.00034
NM_017838.4(NHP2):c.417C>T (p.Tyr139=)	rs567317314	0.00005
NM_017838.4(NHP2):c.337-11C>T	rs1028921372
NM_017838.4(NHP2):c.337-15C>T
NM_017838.4(NHP2):c.337-18C>T
NM_017838.4(NHP2):c.339C>T (p.Asp113=)
NM_017838.4(NHP2):c.366C>G (p.Arg122=)	rs2113463130
NM_017838.4(NHP2):c.378G>A (p.Val126=)	rs1756216301
NM_017838.4(NHP2):c.447G>A (p.Leu149=)	rs754228756
NM_017838.4(NHP2):c.456C>A (p.Pro152=)

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